Variant report

Variant	nsv887879
Chromosome Location	chr7:27175295-27297791
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:4507)
CpG islands
(count:25537)
Chromatin interactive
region (count:231)
LncRNA
region (count:124)
Mature miRNA
region (count: 2)
miRNA target
sites (count:32)

(count:4507 , 50 per page) page: 1 2 3 4 5 6 7 ... 91

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:27175249-27176352	HepG2	liver:	n/a	chr7:27176106-27176122
2	ARID3A	chr7:27200609-27200894	HepG2	liver:	n/a	n/a
3	ARID3A	chr7:27190363-27190815	HepG2	liver:	n/a	n/a
4	ARID3A	chr7:27235933-27236148	K562	blood:	n/a	n/a
5	ARID3A	chr7:27183159-27183652	HepG2	liver:	n/a	n/a
6	ARID3A	chr7:27188911-27189021	HepG2	liver:	n/a	n/a
7	ARID3A	chr7:27250093-27250583	HepG2	liver:	n/a	n/a
8	ARID3A	chr7:27219353-27219704	HepG2	liver:	n/a	n/a
9	ARID3A	chr7:27235883-27236161	HepG2	liver:	n/a	n/a
10	ATF1	chr7:27175464-27175813	K562	blood:	n/a	n/a
11	ATF1	chr7:27176092-27176357	K562	blood:	n/a	n/a
12	ATF2	chr7:27190397-27190797	H1-hESC	embryonic stem cell:	n/a	n/a
13	ATF3	chr7:27195983-27196444	H1-hESC	embryonic stem cell:	n/a	n/a
14	ATF3	chr7:27175370-27176398	A549	lung:	n/a	n/a
15	ATF3	chr7:27196054-27196432	H1-hESC	embryonic stem cell:	n/a	n/a
16	ATF3	chr7:27205081-27205347	H1-hESC	embryonic stem cell:	n/a	chr7:27205195-27205204
17	ATF3	chr7:27200547-27200946	GM12878	blood:	n/a	n/a
18	ATF3	chr7:27205041-27205395	H1-hESC	embryonic stem cell:	n/a	chr7:27205195-27205204
19	ATF3	chr7:27196223-27196345	GM12878	blood:	n/a	n/a
20	ATF3	chr7:27196083-27196467	GM12878	blood:	n/a	n/a
21	BACH1	chr7:27251570-27251658	H1-hESC	embryonic stem cell:	n/a	n/a
22	BACH1	chr7:27282072-27282252	H1-hESC	embryonic stem cell:	n/a	n/a
23	BACH1	chr7:27239932-27239942	H1-hESC	embryonic stem cell:	n/a	n/a
24	BACH1	chr7:27179003-27179135	H1-hESC	embryonic stem cell:	n/a	n/a
25	BACH1	chr7:27260279-27260534	H1-hESC	embryonic stem cell:	n/a	n/a
26	BACH1	chr7:27232791-27232804	H1-hESC	embryonic stem cell:	n/a	n/a
27	BACH1	chr7:27291979-27292164	H1-hESC	embryonic stem cell:	n/a	n/a
28	BACH1	chr7:27182754-27182923	H1-hESC	embryonic stem cell:	n/a	n/a
29	BACH1	chr7:27227265-27227448	H1-hESC	embryonic stem cell:	n/a	n/a
30	BACH1	chr7:27275523-27275711	H1-hESC	embryonic stem cell:	n/a	n/a
31	BACH1	chr7:27200767-27200977	H1-hESC	embryonic stem cell:	n/a	n/a
32	BACH1	chr7:27232517-27232527	H1-hESC	embryonic stem cell:	n/a	n/a
33	BACH1	chr7:27290916-27291310	H1-hESC	embryonic stem cell:	n/a	n/a
34	BATF	chr7:27261054-27261318	GM12878	blood:	n/a	chr7:27261189-27261200
35	BCL3	chr7:27175412-27176007	A549	lung:	n/a	n/a
36	BCL3	chr7:27182969-27183466	A549	lung:	n/a	n/a
37	BCL3	chr7:27175356-27176364	A549	lung:	n/a	n/a
38	BCL3	chr7:27189998-27190798	A549	lung:	n/a	chr7:27190638-27190651 chr7:27190353-27190362
39	BCL3	chr7:27183034-27183631	A549	lung:	n/a	n/a
40	BCL3	chr7:27190403-27191220	A549	lung:	n/a	chr7:27190638-27190651
41	BCLAF1	chr7:27200463-27200972	GM12878	blood:	n/a	n/a
42	BCLAF1	chr7:27200547-27200942	GM12878	blood:	n/a	n/a
43	BHLHE40	chr7:27190423-27190766	HepG2	liver:	n/a	chr7:27190638-27190654 chr7:27190565-27190581 chr7:27190554-27190570
44	BHLHE40	chr7:27200175-27200938	GM12878	blood:	n/a	chr7:27200276-27200292
45	BHLHE40	chr7:27190451-27190791	K562	blood:	n/a	chr7:27190638-27190654 chr7:27190565-27190581 chr7:27190554-27190570
46	BHLHE40	chr7:27219467-27219584	K562	blood:	n/a	n/a
47	BHLHE40	chr7:27190410-27190996	GM12878	blood:	n/a	chr7:27190638-27190654 chr7:27190940-27190956 chr7:27190565-27190581 chr7:27190554-27190570 chr7:27190932-27190948
48	BHLHE40	chr7:27231856-27231876	K562	blood:	n/a	n/a
49	BHLHE40	chr7:27235895-27236179	K562	blood:	n/a	n/a
50	BHLHE40	chr7:27183164-27183646	HepG2	liver:	n/a	chr7:27183378-27183387 chr7:27183378-27183387 chr7:27183372-27183393

(count:25537 , 50 per page) page: 1 2 3 4 5 6 7 ... 511

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:27196153-27196203	NH-A	brain:	n/a
2	chr7:27282431-27282481	LNCaP	prostate:	n/a
3	chr7:27225143-27225193	HCF	heart:	n/a
4	chr7:27281465-27281515	MCF10A-Er-Src	breast:	n/a
5	chr7:27215464-27215514	GM19239	blood:	n/a
6	chr7:27183686-27183736	GM19239	blood:	n/a
7	chr7:27196296-27196346	AG04450	lung:	fetal
8	chr7:27225543-27225593	AG09309	skin:	n/a
9	chr7:27204663-27204713	CMK	blood:	n/a
10	chr7:27209582-27209632	HPAEpiC	pulmonary alveolar:	n/a
11	chr7:27209270-27209320	SK-N-MC	brain:	n/a
12	chr7:27241203-27241253	Hela-S3	cervix:	n/a
13	chr7:27251396-27251446	ovcar-3	ovarian:	n/a
14	chr7:27233480-27233530	HepG2	liver:	n/a
15	chr7:27265463-27265513	SK-N-MC	brain:	n/a
16	chr7:27209195-27209245	SK-N-SH_RA	brain:	n/a
17	chr7:27205504-27205554	HUVEC	blood vessel:	n/a
18	chr7:27223219-27223269	GM19239	blood:	n/a
19	chr7:27184853-27184903	HPAEpiC	pulmonary alveolar:	n/a
20	chr7:27240251-27240301	HRE	kidney:	n/a
21	chr7:27184271-27184321	HPAEpiC	pulmonary alveolar:	n/a
22	chr7:27225897-27225947	HRCEpiC	kidney:	n/a
23	chr7:27260441-27260491	BE2_C	brain:	n/a
24	chr7:27265004-27265054	Hela-S3	cervix:	n/a
25	chr7:27225078-27225128	Hela-S3	cervix:	n/a
26	chr7:27286684-27286734	NT2-D1	testis:	n/a
27	chr7:27213950-27214000	SK-N-MC	brain:	n/a
28	chr7:27238910-27238960	CMK	blood:	n/a
29	chr7:27198311-27198361	HRCEpiC	kidney:	n/a
30	chr7:27191564-27191614	AG09309	skin:	n/a
31	chr7:27196825-27196875	GM19239	blood:	n/a
32	chr7:27227340-27227390	SKMC	muscle:	n/a
33	chr7:27265159-27265209	HNPCEpiC	eye:	n/a
34	chr7:27225058-27225108	ECC-1	luminal epithelium:	n/a
35	chr7:27281346-27281396	Hela-S3	cervix:	n/a
36	chr7:27196296-27196346	NB4	blood:	n/a
37	chr7:27291346-27291396	ProgFib	skin:	n/a
38	chr7:27224954-27225004	NT2-D1	testis:	n/a
39	chr7:27289120-27289170	MCF10A-Er-Src	breast:	n/a
40	chr7:27196153-27196203	NH-A	brain:	n/a
41	chr7:27282431-27282481	LNCaP	prostate:	n/a
42	chr7:27225143-27225193	HCF	heart:	n/a
43	chr7:27281465-27281515	MCF10A-Er-Src	breast:	n/a
44	chr7:27215464-27215514	GM19239	blood:	n/a
45	chr7:27183686-27183736	GM19239	blood:	n/a
46	chr7:27196296-27196346	AG04450	lung:	fetal
47	chr7:27225543-27225593	AG09309	skin:	n/a
48	chr7:27204663-27204713	CMK	blood:	n/a
49	chr7:27209582-27209632	HPAEpiC	pulmonary alveolar:	n/a
50	chr7:27209270-27209320	SK-N-MC	brain:	n/a

(count:231 , 50 per page) page: 1 2 3 4 5

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr21:38738364..38739031-chr7:27212839..27213415,2	Hela-S3	cervix:
2	chr7:27203892..27207242-chr7:27209723..27213341,3	MCF-7	breast:
3	chr7:27223543..27225777-chr7:28060151..28062012,2	MCF-7	breast:
4	chr7:27219637..27221411-chr7:27224788..27226339,2	K562	blood:
5	chr21:36260122..36261007-chr7:27211627..27212520,2	Hela-S3	cervix:
6	chr7:27202105..27204960-chr7:27220530..27223472,3	MCF-7	breast:
7	chr7:27219009..27219512-chr9:131314414..131315243,2	Hela-S3	cervix:
8	chr20:52209640..52210540-chr7:27209024..27209970,2	Hela-S3	cervix:
9	chr7:27190002..27192223-chr7:27198479..27200748,2	MCF-7	breast:
10	chr7:27201693..27204109-chr7:27205812..27207628,2	K562	blood:
11	chr7:27232082..27233586-chr7:27238989..27241639,2	MCF-7	breast:
12	chr7:27263949..27265834-chr7:27269175..27271743,2	K562	blood:
13	chr7:27212193..27213069-chr7:27224455..27225318,2	Hela-S3	cervix:
14	chr7:27178227..27179948-chr7:27181213..27183390,2	MCF-7	breast:
15	chr7:27263949..27265834-chr7:27269175..27271743,2	K562	blood:
16	chr7:27178227..27179948-chr7:27181213..27183390,2	MCF-7	breast:
17	chr7:27219637..27221411-chr7:27224788..27226339,2	K562	blood:
18	chr7:27276853..27279360-chr7:27341599..27343657,2	MCF-7	breast:
19	chr7:26894828..26897181-chr7:27200837..27202990,2	K562	blood:
20	chr5:40834751..40835393-chr7:27227600..27228314,2	Hela-S3	cervix:
21	chr7:27236687..27240147-chr7:27700482..27703881,4	MCF-7	breast:
22	chr7:27258719..27260778-chr7:27263556..27265640,2	K562	blood:
23	chr11:67272436..67272949-chr7:27218842..27219378,2	Hela-S3	cervix:
24	chr1:150533834..150534371-chr7:27224324..27225290,2	Hela-S3	cervix:
25	7:27162022-27164727..7:27216170-27221403	H1-hESC	embryonic stem cell:	embryo
26	chr7:27190581..27191427-chr7:27198722..27199664,2	K562	blood:
27	chr1:155242577..155243301-chr7:27224203..27225069,2	Hela-S3	cervix:
28	chr7:27176401..27178574-chr7:27179994..27182011,2	K562	blood:
29	chr7:26721088..26721712-chr7:27175807..27176765,2	MCF-7	breast:
30	7:27162022-27164727..7:27181770-27195105	H1-hESC	embryonic stem cell:	embryo
31	chr7:27227905..27232079-chr7:27234974..27236957,3	K562	blood:
32	chr7:26903264..26905993-chr7:27172832..27179682,7	MCF-7	breast:
33	chr7:26893161..26894119-chr7:27175695..27176233,2	K562	blood:
34	chr7:27235585..27236283-chr7:27615659..27616283,3	MCF-7	breast:
35	7:27203007-27207968..7:27230275-27238414	H1-hESC	embryonic stem cell:	embryo
36	7:27162022-27164727..7:27203007-27207968	H1-hESC	embryonic stem cell:	embryo
37	chr11:60674246..60674946-chr7:27212653..27213242,2	NB4	blood:
38	7:27181770-27195105..7:27230275-27238414	GM12878	blood:
39	7:27165488-27167947..7:27230275-27238414	H1-hESC	embryonic stem cell:	embryo
40	chr7:26883032..26883964-chr7:27190330..27191296,3	MCF-7	breast:
41	chr14:77278470..77279432-chr7:27214106..27214614,2	Hela-S3	cervix:
42	chr7:27213270..27217080-chr7:27217116..27219781,5	MCF-7	breast:
43	chr7:27249672..27250374-chr7:27369354..27370262,2	MCF-7	breast:
44	7:27176959-27181770..7:27201208-27202386	H1-hESC	embryonic stem cell:	embryo
45	7:27203007-27207968..7:27264409-27279924	H1-hESC	embryonic stem cell:	embryo
46	chr7:27249606..27250151-chr7:27618603..27619596,2	MCF-7	breast:
47	chr7:27211403..27213140-chr7:27217849..27219578,2	MCF-7	breast:
48	chr7:26721768..26723951-chr7:27183878..27185970,2	MCF-7	breast:
49	chr12:54673872..54674764-chr7:27224674..27225242,2	Hela-S3	cervix:
50	chr7:27211408..27213705-chr7:27214550..27217116,2	MCF-7	breast:

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No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-EVX1-1	chr7:27286987-27287020	ENSG00000253324
2	lnc-RP1-170O19.17.1-2	chr7:27282087-27282581	ENSG00000253405.1
3	lnc-RP1-170O19.17.1-2	chr7:27280658-27281629	NONHSAT119723
4	lnc-EVX1-8	chr7:27191913-27192322	ENSG00000254369
5	lnc-EVX1-3	chr7:27240056-27240140	ENSG00000243766.3
6	lnc-EVX1-3	chr7:27240242-27240855	ENSG00000243766
7	lnc-HOXA11-1	chr7:27235769-27235994	NONHSAT119714
8	lnc-EVX1-3	chr7:27240242-27240855	ENSG00000243766
9	lnc-RP1-170O19.17.1-3	chr7:27275467-27275492	XLOC_006391
10	lnc-EVX1-8	chr7:27191913-27192345	ENSG00000254369
11	lnc-EVX1-3	chr7:27240242-27242441	ENSG00000243766
12	lnc-HOXA4-1	chr7:27179702-27179805	NONHSAT119681
13	lnc-EVX1-3	chr7:27240056-27240140	ENSG00000243766
14	lnc-EVX1-8	chr7:27191194-27191300	ENSG00000254369
15	lnc-EVX1-3	chr7:27240242-27242257	NR_037843
16	lnc-EVX1-3	chr7:27244331-27246878	ENSG00000243766
17	lnc-HOXA7-1	chr7:27192717-27192967	NONHSAT119689
18	lnc-EVX1-3	chr7:27240040-27240140	ENSG00000243766
19	lnc-EVX1-3	chr7:27241461-27242257	ENSG00000243766
20	lnc-EVX1-3	chr7:27240242-27240855	ENSG00000243766
21	lnc-EVX1-3	chr7:27241461-27242257	ENSG00000243766
22	lnc-EVX1-5	chr7:27228220-27228912	XLOC_006025
23	lnc-EVX1-3	chr7:27240242-27241442	ENSG00000243766.3
24	lnc-EVX1-3	chr7:27240242-27241306	ENSG00000243766
25	lnc-EVX1-3	chr7:27240056-27240140	ENSG00000243766
26	lnc-RP1-170O19.17.1-2	chr7:27281534-27281629	ENSG00000253405.1
27	lnc-HOXA4-1	chr7:27179702-27179844	NONHSAT119671
28	lnc-EVX1-3	chr7:27240040-27240140	ENSG00000243766
29	lnc-HOXA13-4	chr7:27247349-27247372	NONHSAT119719
30	lnc-EVX1-3	chr7:27241461-27242257	ENSG00000243766
31	lnc-EVX1-8	chr7:27189671-27191300	ENSG00000254369
32	lnc-EVX1-5	chr7:27227693-27228912	NONHSAT119711
33	lnc-EVX1-3	chr7:27240056-27240140	ENSG00000243766
34	lnc-RP1-170O19.17.1-2	chr7:27286580-27286848	ENSG00000253405.1
35	lnc-EVX1-5	chr7:27225739-27225882	ENSG00000240990.4
36	lnc-EVX1-8	chr7:27191913-27192195	ENSG00000254369
37	lnc-RP1-170O19.17.1-2	chr7:27281569-27281629	ENSG00000253405.1
38	lnc-EVX1-8	chr7:27187102-27187205	ENSG00000254369
39	lnc-HOXA7-1	chr7:27199288-27199592	NONHSAT119689
40	lnc-EVX1-7	chr7:27210927-27211534	ENSG00000253187.2
41	lnc-EVX1-3	chr7:27244331-27246878	ENSG00000243766
42	lnc-RP1-170O19.17.1-3	chr7:27268955-27269542	XLOC_006391
43	lnc-EVX1-1	chr7:27289767-27290112	ENSG00000253324
44	lnc-RP1-170O19.17.1-2	chr7:27282249-27282355	ENSG00000253405.1
45	lnc-EVX1-5	chr7:27225153-27225882	ENSG00000240990.4
46	lnc-HOXA4-1	chr7:27191907-27192217	ENSG00000272801.1
47	lnc-EVX1-3	chr7:27240242-27241306	ENSG00000243766
48	lnc-HOXA13-3	chr7:27234405-27235219	NONHSAT119713
49	lnc-EVX1-3	chr7:27238194-27238360	ENSG00000243766
50	lnc-EVX1-3	chr7:27240242-27241306	ENSG00000243766

miRNA name	Chromosome Location	mirBase accession
hsa-miR-196b-3p	chr7:27209112-27209133	MIMAT0009201
hsa-miR-196b-5p	chr7:27209147-27209168	MIMAT0001080

(count:32 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	HOXA10	hsa-miR-320a	chr7:27210862-27210855
2	HOXA5	hsa-miR-183-5p	chr7:27181297-27181318
3	HOXA7	hsa-miR-196a-5p	chr7:27194188-27194181
4	HOXA5	hsa-miR-130a-3p	chr7:27181097-27181091
5	HOXA5	hsa-miR-196a-5p	chr7:27181006-27181027
6	HOXA11	hsa-miR-30d-5p	chr7:27221235-27221256
7	HOXA5	hsa-miR-19a-3p	chr7:27180870-27180864
8	HOXA7	hsa-miR-196a-5p	chr7:27194055-27194048
9	HOXA9	hsa-miR-18a-5p	chr7:27202488-27202510
10	HOXA7	hsa-miR-196a-5p	chr7:27194219-27194240
11	HOXA10	hsa-miR-320a	chr7:27210218-27210239
12	HOXA5	hsa-miR-130b-3p	chr7:27181091-27181114
13	HOXA7	hsa-miR-196a-5p	chr7:27194067-27194095
14	HOXA7	hsa-miR-196a-5p	chr7:27194182-27194203
15	HOXA10	hsa-miR-320a	chr7:27210856-27210877
16	HOXA5	hsa-miR-196a-5p	chr7:27181012-27181005
17	HOXA9	hsa-miR-26b-5p	chr7:27202776-27202769
18	HOXA7	hsa-miR-196a-5p	chr7:27194073-27194066
19	HOXA5	hsa-miR-19b-3p	chr7:27180870-27180864
20	HOXA10	hsa-miR-204-5p	chr7:27210459-27210477
21	HOXA5	hsa-miR-340-5p	chr7:27181203-27181224
22	HOXA11	hsa-miR-30d-5p	chr7:27221241-27221234
23	HOXA9	hsa-miR-26b-5p	chr7:27202770-27202790
24	HOXA9	hsa-miR-33a-5p	chr7:27202861-27202881
25	HOXA7	hsa-miR-196a-5p	chr7:27194049-27194070
26	HOXA9	hsa-miR-340-5p	chr7:27202866-27202887
27	HOXA9	hsa-miR-96-5p	chr7:27202080-27202102
28	HOXA5	hsa-miR-130a-3p	chr7:27181091-27181114
29	HOXA9	hsa-miR-324-5p	chr7:27202513-27202535
30	HOXA11	hsa-miR-335-5p	chr7:27221418-27221441
31	HOXA5	hsa-miR-130b-3p	chr7:27181097-27181091
32	HOXA7	hsa-miR-196a-5p	chr7:27194225-27194218

Variant related genes	Relation type
HOXA11-AS	TF binding region
ENSG00000253308	TF binding region
HOXA7	TF binding region
HOXA11	TF binding region
EVX1-AS	TF binding region
HOXA10-AS	TF binding region
ENSG00000270182	TF binding region
ENSG00000273433	TF binding region
HOXA6	TF binding region
ENSG00000253508	TF binding region
HOXA9	TF binding region
ENSG00000272801	TF binding region
HOXA5	TF binding region
HOTTIP	TF binding region
HOXA10	TF binding region
HOXA-AS3	TF binding region
ENSG00000257184	TF binding region
HOXA13	TF binding region
EVX1	TF binding region
HOXA3	TF binding region
HOXA4	TF binding region
MIR196B	TF binding region
HOXA11-AS	CpG island
ENSG00000253308	CpG island
HOXA7	CpG island
HOXA11	CpG island
EVX1-AS	CpG island
HOXA10-AS	CpG island
ENSG00000270182	CpG island
ENSG00000273433	CpG island
HOXA6	CpG island
ENSG00000253508	CpG island
HOXA9	CpG island
ENSG00000272801	CpG island
HOXA5	CpG island
HOTTIP	CpG island
HOXA10	CpG island
HOXA-AS3	CpG island
ENSG00000257184	CpG island
HOXA13	CpG island
EVX1	CpG island
HOXA3	CpG island
HOXA4	CpG island
MIR196B	CpG island
ENSG00000272801	chromatin interactions
ENSG00000078399	chromatin interactions
ENSG00000139168	chromatin interactions
ENSG00000066933	chromatin interactions
ENSG00000253187	chromatin interactions
ENSG00000266055	chromatin interactions
ENSG00000261423	chromatin interactions
ENSG00000176444	chromatin interactions
ENSG00000078808	chromatin interactions
ENSG00000130826	chromatin interactions
ENSG00000094916	chromatin interactions
ENSG00000005020	chromatin interactions
ENSG00000176853	chromatin interactions
ENSG00000270103	chromatin interactions
ENSG00000120875	chromatin interactions
ENSG00000177548	chromatin interactions
ENSG00000165675	chromatin interactions
ENSG00000100726	chromatin interactions
ENSG00000133316	chromatin interactions
ENSG00000196547	chromatin interactions
ENSG00000123358	chromatin interactions
ENSG00000135486	chromatin interactions
ENSG00000106004	chromatin interactions
ENSG00000106006	chromatin interactions
ENSG00000106038	chromatin interactions
ENSG00000151876	chromatin interactions
ENSG00000254369	chromatin interactions
ENSG00000166192	chromatin interactions
ENSG00000134283	chromatin interactions
ENSG00000253308	chromatin interactions
ENSG00000201558	chromatin interactions
ENSG00000110697	chromatin interactions
ENSG00000105991	chromatin interactions
ENSG00000158710	chromatin interactions
ENSG00000188825	chromatin interactions
ENSG00000253552	chromatin interactions
ENSG00000233429	chromatin interactions
ENSG00000243766	chromatin interactions
ENSG00000270022	chromatin interactions
ENSG00000115310	chromatin interactions
ENSG00000197576	chromatin interactions
ENSG00000170100	chromatin interactions
ENSG00000240990	chromatin interactions
ENSG00000113575	chromatin interactions
ENSG00000266751	chromatin interactions
ENSG00000013523	chromatin interactions
ENSG00000197694	chromatin interactions
ENSG00000122566	chromatin interactions
ENSG00000176022	chromatin interactions
ENSG00000081154	chromatin interactions
ENSG00000106031	chromatin interactions
ENSG00000214869	chromatin interactions
ENSG00000226059	chromatin interactions
ENSG00000064933	chromatin interactions
ENSG00000228395	chromatin interactions
ENSG00000272772	chromatin interactions
ENSG00000259877	chromatin interactions
ENSG00000145592	chromatin interactions
ENSG00000122565	chromatin interactions
ENSG00000203804	chromatin interactions
ENSG00000122592	chromatin interactions
ENSG00000119787	chromatin interactions
ENSG00000273433	chromatin interactions
ENSG00000253293	chromatin interactions
ENSG00000106049	chromatin interactions
ENSG00000239305	chromatin interactions
ENSG00000213786	chromatin interactions
ENSG00000100227	chromatin interactions
ENSG00000257184	chromatin interactions
ENSG00000113407	chromatin interactions
ENSG00000005073	chromatin interactions
ENSG00000253405	chromatin interactions
ENSG00000151240	chromatin interactions
ENSG00000153814	chromatin interactions
ENSG00000187555	chromatin interactions
ENSG00000159216	chromatin interactions
ENSG00000270177	chromatin interactions
ENSG00000136045	chromatin interactions
ENSG00000105997	chromatin interactions
ENSG00000257052	chromatin interactions
ENSG00000143384	chromatin interactions
ENSG00000266559	chromatin interactions
ENSG00000128699	chromatin interactions
ENSG00000171940	chromatin interactions
ENSG00000253508	chromatin interactions
ENSG00000168374	chromatin interactions
HOXA9	lncRNA
HOXA7	lncRNA
HOXA10	lncRNA
HOXA11	lncRNA
HOXA13	lncRNA
BUB1	Mature miRNA region
MT-CO3	Mature miRNA region
TXLNA	Mature miRNA region
TXNDC5	Mature miRNA region
CACNB3	Mature miRNA region
GNB2L1	Mature miRNA region
MAPRE1	Mature miRNA region
ATF4	Mature miRNA region
PDE12	Mature miRNA region
ALDOA	Mature miRNA region
MSH6	Mature miRNA region
WHSC1L1	Mature miRNA region
PRKACA	Mature miRNA region
BCL2	Mature miRNA region
IARS	Mature miRNA region
PALD1	Mature miRNA region
GPS1	Mature miRNA region
BCAR3	Mature miRNA region
HOXB8	Mature miRNA region
CDK5R1	Mature miRNA region
TUBB	Mature miRNA region
RPS3	Mature miRNA region
TLE3	Mature miRNA region
MEPCE	Mature miRNA region
HSD17B10	Mature miRNA region
HOXC8	Mature miRNA region
RRP1B	Mature miRNA region
CD8A	Mature miRNA region
LAMB2	Mature miRNA region
SLC6A15	Mature miRNA region
SLC23A2	Mature miRNA region
MRPS35	Mature miRNA region
MAT2A	Mature miRNA region
REEP5	Mature miRNA region
MRPS26	Mature miRNA region
SNX9	Mature miRNA region
TRA2A	Mature miRNA region
MT-ATP6	Mature miRNA region
CKB	Mature miRNA region
PAXBP1	Mature miRNA region
AJUBA	Mature miRNA region
BEST3	Mature miRNA region
MFHAS1	Mature miRNA region
RTF1	Mature miRNA region
KMT2D	Mature miRNA region
LHX2	Mature miRNA region
HTR1D	Mature miRNA region
CHD2	Mature miRNA region
MT-ND5	Mature miRNA region
HERC2	Mature miRNA region
TMTC3	miRNA target sites
MOBKL1A	miRNA target sites
HMGB2	miRNA target sites
OSBPL9	miRNA target sites
RNF34	miRNA target sites
TBC1D1	miRNA target sites
DICER1	miRNA target sites
NFIA	miRNA target sites
SPAG1	miRNA target sites
CCNL1	miRNA target sites
FAM136A	miRNA target sites
UNG	miRNA target sites
PLAG1	miRNA target sites

Extended variants
information (count: 4742 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:4742 , 50 per page) page: 1 2 3 4 5 6 7 ... 95

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12533947	chr7:27175295-27175296	Enhancers Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	13 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs189829974	chr7:27175303-27175304	Enhancers Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
3	rs569149741	chr7:27175314-27175315	Enhancers Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
4	rs112835202	chr7:27175355-27175356	Enhancers Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
5	rs538083759	chr7:27175453-27175454	Enhancers Flanking Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
6	rs551614148	chr7:27175517-27175518	Enhancers Flanking Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
7	rs140534874	chr7:27175523-27175524	Enhancers Flanking Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
8	rs533675499	chr7:27175540-27175541	Enhancers Flanking Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
9	rs111453426	chr7:27175587-27175588	Enhancers Flanking Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
10	rs575508608	chr7:27175604-27175605	Enhancers Bivalent Enhancer Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Active TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
11	rs553798787	chr7:27175634-27175635	Enhancers Bivalent Enhancer Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Active TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
12	rs544695285	chr7:27175636-27175637	Enhancers Bivalent Enhancer Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Active TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
13	rs573589980	chr7:27175644-27175645	Enhancers Bivalent Enhancer Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Active TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
14	rs536222485	chr7:27175670-27175671	Enhancers Bivalent Enhancer Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Active TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
15	rs561271431	chr7:27175682-27175683	Enhancers Bivalent Enhancer Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Active TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
16	rs17427714	chr7:27175698-27175699	Enhancers Bivalent Enhancer Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Active TSS	TF binding region Chromatin interactive region	12 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs182198339	chr7:27175761-27175762	Enhancers Bivalent Enhancer Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Active TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
18	rs143439513	chr7:27175770-27175771	Enhancers Bivalent Enhancer Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Active TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
19	rs77954684	chr7:27175798-27175799	Enhancers Bivalent Enhancer Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Active TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
20	rs544461437	chr7:27175803-27175804	Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Weak transcription Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
21	rs146756769	chr7:27175808-27175809	Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Weak transcription Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
22	rs78959477	chr7:27175815-27175816	Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Weak transcription Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
23	rs185627652	chr7:27175838-27175839	Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Weak transcription Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
24	rs35013636	chr7:27175840-27175841	Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Weak transcription Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
25	rs140454137	chr7:27175887-27175888	Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Weak transcription Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
26	rs559892282	chr7:27175889-27175890	Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Weak transcription Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
27	rs79208955	chr7:27175904-27175905	Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Weak transcription Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
28	rs529296662	chr7:27175945-27175946	Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Weak transcription Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
29	rs543039404	chr7:27175958-27175959	Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Weak transcription Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
30	rs143546071	chr7:27175995-27175996	Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Weak transcription Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
31	rs531642050	chr7:27176001-27176002	Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Active TSS Genic enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
32	rs552016671	chr7:27176039-27176040	Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Active TSS Genic enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
33	rs377518169	chr7:27176066-27176067	Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Active TSS Genic enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
34	rs17500806	chr7:27176100-27176101	Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Active TSS Genic enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS	TF binding region Chromatin interactive region	12 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs148042509	chr7:27176101-27176102	Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Active TSS Genic enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
36	rs527468427	chr7:27176102-27176103	Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Active TSS Genic enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
37	rs191452710	chr7:27176125-27176126	Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Active TSS Genic enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
38	rs567352412	chr7:27176194-27176195	Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Active TSS Genic enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
39	rs373388648	chr7:27176251-27176252	Enhancers Bivalent/Poised TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Weak transcription Active TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
40	rs535910288	chr7:27176265-27176266	Enhancers Bivalent/Poised TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Weak transcription Active TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
41	rs555750314	chr7:27176266-27176267	Enhancers Bivalent/Poised TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Weak transcription Active TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
42	rs569262146	chr7:27176270-27176271	Enhancers Bivalent/Poised TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Weak transcription Active TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
43	rs538169226	chr7:27176283-27176284	Enhancers Bivalent/Poised TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Weak transcription Active TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
44	rs557995043	chr7:27176346-27176347	Enhancers Bivalent/Poised TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Weak transcription Active TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
45	rs182785851	chr7:27176389-27176390	Enhancers Bivalent/Poised TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Weak transcription Active TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
46	rs376652208	chr7:27176469-27176470	Enhancers Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Genic enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
47	rs140764269	chr7:27176472-27176473	Enhancers Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Genic enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
48	rs17427721	chr7:27176494-27176495	Enhancers Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Genic enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region	10 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs574068468	chr7:27176507-27176508	Enhancers Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Genic enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
50	rs543099094	chr7:27176539-27176540	Enhancers Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Genic enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:86)

Disease	PMID	Source
Urothelial carcinoma	18382360	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Biliary cancer	19435499	CNVD
Cancer	16751803	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	17387387	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	18923191	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
colon cancer	17210682	CNVD
Lung adenocarcinoma	21810691	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Colorectal cancer	19359472	CNVD
Hypothalamic hamartomas	18252217	CNVD
Human rectal carcinomas	16397240	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Medulloblastoma	18056178	CNVD
Basal cell lymphoma	17170743	CNVD
Ewing''s sarcoma	21437220	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Autism	22495311	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Cancer	21637783	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	16397240	CNVD
Non-small cell lung cancer	21829676	CNVD
Glioblastoma multiforme	17002787	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Glioblastoma multiforme	18628472	CNVD
Non-syndromic sensorineural hearing loss	22570644	CNVD
Cancer	21183584	CNVD
abnormal development	18461090	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	21785460	CNVD
Follicular lymphoma	20505157	CNVD
Williams-beuren syndrome	22470819	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	21645411	CNVD
Lung adenocarcinoma	17086460	CNVD
Colorectal cancer	19455253	CNVD
Lung cancer	17086460	CNVD
Breast cancer	18852474	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	22522925	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:7227 , 50 per page) page: 1 2 3 4 5 6 7 ... 145

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:27171200-27175400	Enhancers	NHLF	lung
2	chr7:27171200-27175600	Enhancers	Fetal Stomach	stomach
3	chr7:27171200-27175800	Enhancers	Fetal Intestine Large	intestine
4	chr7:27171200-27176400	Weak transcription	Lung	lung
5	chr7:27171200-27181400	Weak transcription	Esophagus	oesophagus
6	chr7:27171400-27175400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr7:27171400-27175800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr7:27171400-27175800	Weak transcription	HSMMtube	muscle
9	chr7:27172600-27178400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr7:27173000-27175600	Enhancers	Duodenum Smooth Muscle	Duodenum
11	chr7:27173000-27175800	Genic enhancers	Fetal Muscle Leg	muscle
12	chr7:27173000-27176400	Enhancers	Adipose Nuclei	Adipose
13	chr7:27173000-27176800	Enhancers	NHEK	skin
14	chr7:27173200-27175600	Enhancers	HMEC	breast
15	chr7:27173400-27175400	Enhancers	Breast Myoepithelial Primary Cells	Breast
16	chr7:27173400-27175800	Enhancers	Osteobl	bone
17	chr7:27173400-27177600	Enhancers	Muscle Satellite Cultured Cells	--
18	chr7:27173600-27175600	Bivalent Enhancer	Primary neutrophils fromperipheralblood	blood
19	chr7:27173600-27177600	Enhancers	Primary hematopoietic stem cells	blood
20	chr7:27173800-27175400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
21	chr7:27173800-27175400	Enhancers	Rectal Mucosa Donor 31	rectum
22	chr7:27173800-27175800	Enhancers	NHDF-Ad	bronchial
23	chr7:27173800-27176400	Weak transcription	Psoas Muscle	Psoas
24	chr7:27173800-27178400	Enhancers	Fetal Intestine Small	intestine
25	chr7:27173800-27178600	Enhancers	Colon Smooth Muscle	Colon
26	chr7:27173800-27179200	Genic enhancers	Primary hematopoietic stem cells short term culture	blood
27	chr7:27174000-27175600	Enhancers	Monocytes-CD14+_RO01746	blood
28	chr7:27174000-27175800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
29	chr7:27174000-27175800	Transcr. at gene 5' and 3'	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr7:27174000-27176000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr7:27174200-27175400	Enhancers	HepG2	liver
32	chr7:27174200-27175600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
33	chr7:27174200-27175600	Enhancers	Primary T cells from cord blood	blood
34	chr7:27174400-27175400	Bivalent Enhancer	Fetal Lung	lung
35	chr7:27174400-27175400	Enhancers	HUVEC	blood vessel
36	chr7:27174400-27175600	Weak transcription	Colonic Mucosa	Colon
37	chr7:27174400-27175600	Weak transcription	Sigmoid Colon	Sigmoid Colon
38	chr7:27174400-27175600	Weak transcription	Skeletal Muscle Female	skeletal muscle
39	chr7:27174600-27175400	Genic enhancers	Fetal Kidney	kidney
40	chr7:27174600-27175800	Bivalent Enhancer	Duodenum Mucosa	Duodenum
41	chr7:27174800-27175400	Enhancers	Stomach Smooth Muscle	stomach
42	chr7:27174800-27175600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
43	chr7:27174800-27175600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
44	chr7:27174800-27175800	Weak transcription	Skeletal Muscle Male	skeletal muscle
45	chr7:27174800-27175800	Weak transcription	HSMM	muscle
46	chr7:27175000-27175400	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
47	chr7:27175000-27175600	Bivalent Enhancer	Primary T killer memory cells from peripheral blood	blood
48	chr7:27175000-27175800	Enhancers	Rectal Mucosa Donor 29	rectum
49	chr7:27175000-27176800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
50	chr7:27175000-27177200	Bivalent Enhancer	Fetal Thymus	thymus

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