Variant report

Variant	esv2755349
Chromosome Location	chr5:115384101-115733101
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2603)
CpG islands
(count:1649)
Chromatin interactive
region (count:92)
LncRNA
region (count:24)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2603 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:115403795-115404079	K562	blood:	n/a	n/a
2	ARID3A	chr5:115420927-115421286	HepG2	liver:	n/a	n/a
3	ARID3A	chr5:115473442-115473811	K562	blood:	n/a	n/a
4	ARID3A	chr5:115567073-115567351	HepG2	liver:	n/a	n/a
5	ARID3A	chr5:115410898-115411078	K562	blood:	n/a	n/a
6	ARID3A	chr5:115420453-115420725	HepG2	liver:	n/a	n/a
7	ATF1	chr5:115705390-115705679	K562	blood:	n/a	n/a
8	ATF1	chr5:115707706-115707979	K562	blood:	n/a	n/a
9	ATF1	chr5:115614176-115614178	K562	blood:	n/a	n/a
10	ATF1	chr5:115694484-115694974	K562	blood:	n/a	n/a
11	ATF1	chr5:115700581-115701001	K562	blood:	n/a	n/a
12	ATF1	chr5:115426098-115426398	K562	blood:	n/a	n/a
13	ATF1	chr5:115420602-115421231	K562	blood:	n/a	n/a
14	ATF1	chr5:115410893-115411113	K562	blood:	n/a	n/a
15	ATF1	chr5:115679669-115679868	K562	blood:	n/a	n/a
16	ATF1	chr5:115394162-115394612	K562	blood:	n/a	n/a
17	ATF2	chr5:115412006-115412690	GM12878	blood:	n/a	n/a
18	ATF2	chr5:115694460-115695182	GM12878	blood:	n/a	n/a
19	ATF2	chr5:115420612-115421281	GM12878	blood:	n/a	n/a
20	ATF2	chr5:115700598-115701276	GM12878	blood:	n/a	n/a
21	ATF2	chr5:115411962-115412753	GM12878	blood:	n/a	n/a
22	ATF2	chr5:115697348-115697730	H1-hESC	embryonic stem cell:	n/a	n/a
23	ATF2	chr5:115470974-115471521	GM12878	blood:	n/a	n/a
24	ATF2	chr5:115694360-115694992	GM12878	blood:	n/a	n/a
25	ATF2	chr5:115420461-115421375	GM12878	blood:	n/a	n/a
26	ATF3	chr5:115420549-115421037	A549	lung:	n/a	n/a
27	ATF3	chr5:115420907-115421300	K562	blood:	n/a	n/a
28	ATF3	chr5:115420925-115421272	GM12878	blood:	n/a	n/a
29	BACH1	chr5:115573174-115573254	H1-hESC	embryonic stem cell:	n/a	n/a
30	BACH1	chr5:115394268-115394429	K562	blood:	n/a	n/a
31	BACH1	chr5:115679748-115679880	H1-hESC	embryonic stem cell:	n/a	n/a
32	BACH1	chr5:115420883-115421200	H1-hESC	embryonic stem cell:	n/a	n/a
33	BACH1	chr5:115697108-115697625	H1-hESC	embryonic stem cell:	n/a	n/a
34	BATF	chr5:115609200-115609492	GM12878	blood:	n/a	chr5:115609356-115609366 chr5:115609352-115609362 chr5:115609355-115609366
35	BATF	chr5:115412087-115412508	GM12878	blood:	n/a	n/a
36	BATF	chr5:115411990-115412543	GM12878	blood:	n/a	n/a
37	BATF	chr5:115700938-115701321	GM12878	blood:	n/a	n/a
38	BATF	chr5:115609206-115609493	GM12878	blood:	n/a	chr5:115609356-115609366 chr5:115609352-115609362 chr5:115609355-115609366
39	BATF	chr5:115694520-115694822	GM12878	blood:	n/a	n/a
40	BATF	chr5:115710093-115710344	GM12878	blood:	n/a	n/a
41	BATF	chr5:115708897-115709253	GM12878	blood:	n/a	chr5:115709039-115709049 chr5:115709038-115709049
42	BATF	chr5:115700697-115701341	GM12878	blood:	n/a	chr5:115700750-115700759
43	BCL11A	chr5:115694504-115694827	GM12878	blood:	n/a	n/a
44	BCL11A	chr5:115700601-115701297	GM12878	blood:	n/a	n/a
45	BCL11A	chr5:115471127-115471339	GM12878	blood:	n/a	n/a
46	BCL11A	chr5:115420926-115421266	GM12878	blood:	n/a	chr5:115421155-115421164
47	BCL11A	chr5:115694461-115694921	GM12878	blood:	n/a	n/a
48	BCL11A	chr5:115412115-115412634	GM12878	blood:	n/a	chr5:115412389-115412398
49	BCL11A	chr5:115412199-115412507	GM12878	blood:	n/a	chr5:115412389-115412398
50	BCL3	chr5:115412069-115412535	GM12878	blood:	n/a	chr5:115412389-115412398

(count:1649 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:115387951-115388001	BE2_C	brain:	n/a
2	chr5:115705963-115706013	Caco-2	colon:	n/a
3	chr5:115387951-115388001	BE2_C	brain:	n/a
4	chr5:115705963-115706013	Caco-2	colon:	n/a
5	chr5:115420814-115420864	HEEpiC	esophagus:	n/a
6	chr5:115697214-115697264	NHBE	bronchial:	n/a
7	chr5:115387984-115388034	HEK293	kidney:	embryo
8	chr5:115420761-115420811	GM19239	blood:	n/a
9	chr5:115421194-115421244	HUVEC	blood vessel:	n/a
10	chr5:115425060-115425110	NT2-D1	testis:	n/a
11	chr5:115418530-115418580	AG04449	skin:	fetal
12	chr5:115639617-115639667	ovcar-3	ovarian:	n/a
13	chr5:115724285-115724335	H1-hESC	embryonic stem cell:	embryo
14	chr5:115450589-115450639	NT2-D1	testis:	n/a
15	chr5:115693708-115693758	HepG2	liver:	n/a
16	chr5:115697214-115697264	HEK293	kidney:	embryo
17	chr5:115697446-115697496	ECC-1	luminal epithelium:	n/a
18	chr5:115418530-115418580	AG09309	skin:	n/a
19	chr5:115697214-115697264	Hepatocyte	liver:	n/a
20	chr5:115420544-115420594	ECC-1	luminal epithelium:	n/a
21	chr5:115693708-115693758	GM12891	blood:	n/a
22	chr5:115724285-115724335	GM06990	blood:	n/a
23	chr5:115421194-115421244	GM12891	blood:	n/a
24	chr5:115697696-115697746	HRPEpiC	eye:	n/a
25	chr5:115712252-115712302	LNCaP	prostate:	n/a
26	chr5:115420544-115420594	SAEC	small airway:	n/a
27	chr5:115724285-115724335	HRPEpiC	eye:	n/a
28	chr5:115420582-115420632	PANC-1	pancreas:	n/a
29	chr5:115420582-115420632	T-47D	breast:	n/a
30	chr5:115421194-115421244	NHBE	bronchial:	n/a
31	chr5:115421194-115421244	NH-A	brain:	n/a
32	chr5:115420544-115420594	AG09309	skin:	n/a
33	chr5:115421152-115421202	HCT-116	colon:	n/a
34	chr5:115425060-115425110	AG04449	skin:	fetal
35	chr5:115387951-115388001	AG04449	skin:	fetal
36	chr5:115418530-115418580	HAEpiC	amniotic membrane:	n/a
37	chr5:115697446-115697496	BE2_C	brain:	n/a
38	chr5:115697214-115697264	AoSMC	blood vessel:	n/a
39	chr5:115599680-115599730	HMEC	breast:	n/a
40	chr5:115724285-115724335	HUVEC	blood vessel:	n/a
41	chr5:115421035-115421085	NHDF-neo	bronchial:	n/a
42	chr5:115421152-115421202	NHBE	bronchial:	n/a
43	chr5:115420814-115420864	AG09319	gingival:	n/a
44	chr5:115639617-115639667	T-47D	breast:	n/a
45	chr5:115418530-115418580	HMEC	breast:	n/a
46	chr5:115387951-115388001	AG09319	gingival:	n/a
47	chr5:115697588-115697638	AG10803	skin:	n/a
48	chr5:115387951-115388001	HepG2	liver:	n/a
49	chr5:115419881-115419931	AG04450	lung:	fetal
50	chr5:115420582-115420632	Hela-S3	cervix:	n/a

(count:92 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr5:115420095..115422778-chr5:115430686..115433212,3	MCF-7	breast:
2	chr5:115177015..115179299-chr5:115418616..115421272,3	K562	blood:
3	chr5:115402359..115404249-chr5:115418524..115420135,2	K562	blood:
4	chr5:115418449..115420927-chr5:115462896..115464541,2	K562	blood:
5	chr5:115408709..115410572-chr5:115414049..115415857,2	MCF-7	breast:
6	chr5:115523919..115526832-chr5:115553749..115555427,2	MCF-7	breast:
7	chr5:115413293..115416934-chr5:115419212..115422160,5	MCF-7	breast:
8	chr5:115418515..115421238-chr5:115424044..115426973,2	MCF-7	breast:
9	chr5:115573428..115574084-chr5:115607901..115608709,2	MCF-7	breast:
10	chr5:115176142..115179137-chr5:115398497..115401222,2	MCF-7	breast:
11	chr5:115419680..115422174-chr5:115452572..115455057,2	MCF-7	breast:
12	chr5:114970518..114971324-chr5:115403283..115404403,4	K562	blood:
13	chr5:115379424..115381506-chr5:115383490..115386090,2	K562	blood:
14	chr11:21157468..21158972-chr5:115430256..115431756,2	MCF-7	breast:
15	chr5:115647669..115649812-chr5:115683571..115685304,2	K562	blood:
16	chr5:115418515..115421238-chr5:115424044..115426973,2	MCF-7	breast:
17	chr5:115420483..115422692-chr5:115428367..115432405,4	MCF-7	breast:
18	chr5:115692236..115694986-chr5:115697167..115699493,2	MCF-7	breast:
19	chr5:115711711..115714418-chr5:115718644..115720507,2	K562	blood:
20	chr5:115477963..115480064-chr5:115480486..115482717,2	K562	blood:
21	chr5:115418542..115422487-chr5:115423504..115427625,5	MCF-7	breast:
22	chr5:115418695..115421478-chr5:115430804..115432304,2	K562	blood:
23	chr5:115512590..115515778-chr5:115516651..115520258,3	MCF-7	breast:
24	chr5:115423355..115429096-chr5:115429659..115434037,6	K562	blood:
25	chr5:115431884..115434416-chr5:115451435..115454225,2	K562	blood:
26	chr5:115693595..115697814-chr5:115698835..115703078,5	K562	blood:
27	chr5:115473639..115474170-chr5:115607611..115608509,2	MCF-7	breast:
28	chr5:115177392..115178980-chr5:115419410..115421076,2	MCF-7	breast:
29	chr5:115704428..115706706-chr5:115709540..115711421,2	MCF-7	breast:
30	chr16:3073983..3074533-chr5:115420524..115421124,2	Hela-S3	cervix:
31	chr5:115420205..115422091-chr5:138940296..138941951,2	MCF-7	breast:
32	chr5:115402497..115406004-chr5:115407456..115411248,3	K562	blood:
33	chr5:115714143..115716016-chr5:115739014..115740918,2	K562	blood:
34	chr5:115405163..115410303-chr5:115417488..115422793,7	K562	blood:
35	chr5:115379944..115382363-chr5:115409164..115412094,2	MCF-7	breast:
36	chr5:115632385..115634405-chr5:115635053..115637473,2	K562	blood:
37	chr5:115473639..115474170-chr5:115607611..115608509,2	MCF-7	breast:
38	chr5:115473058..115473763-chr5:115624723..115625238,2	MCF-7	breast:
39	chr5:115632385..115634405-chr5:115635053..115637473,2	K562	blood:
40	chr5:114960090..114964183-chr5:115419193..115421485,4	MCF-7	breast:
41	chr5:114970091..114970643-chr5:115403493..115404412,2	MCF-7	breast:
42	chr5:115693595..115697814-chr5:115698835..115703078,5	K562	blood:
43	chr4:184425377..184425891-chr5:115420080..115420819,2	Hela-S3	cervix:
44	chr5:115607181..115609929-chr5:115613382..115615949,2	K562	blood:
45	chr5:115630950..115633524-chr5:115633964..115636710,2	MCF-7	breast:
46	chr5:115704428..115706706-chr5:115709540..115711421,2	MCF-7	breast:
47	chr5:115402359..115404249-chr5:115418524..115420135,2	K562	blood:
48	chr17:39845051..39845605-chr5:115420384..115421275,2	Hela-S3	cervix:
49	chr5:115685651..115688638-chr5:115690874..115693480,2	K562	blood:
50	chr5:115374690..115376752-chr5:115422929..115424884,2	K562	blood:

(count:24 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-COMMD10-6	chr5:115667126-115667860	l_3000_chr5:115661715-115668338_thyroid
2	lnc-LVRN.1-4	chr5:115628154-115628257	NONHSAT103358
3	lnc-ATG12-5	chr5:115419504-115421113	ENSG00000271918.1
4	lnc-COMMD10-6	chr5:115667915-115668338	l_3000_chr5:115661715-115668338_thyroid
5	lnc-ATG12-4	chr5:115413807-115414267	ENSG00000272265.1
6	lnc-LVRN.1-4	chr5:115639227-115639380	NONHSAT103358
7	lnc-LVRN.1-4	chr5:115643332-115643482	NONHSAT103359
8	lnc-SEMA6A-1	chr5:115703113-115706170	NONHSAT103361
9	lnc-SEMA6A-1	chr5:115708676-115708786	NONHSAT103361
10	lnc-SEMA6A-1	chr5:115710179-115710267	ENSG00000249280
11	lnc-SEMA6A-7	chr5:115553723-115553992	NONHSAT103356
12	lnc-SEMA6A-1	chr5:115708676-115708786	ENSG00000249280
13	lnc-LVRN.1-4	chr5:115641553-115642622	NONHSAT103359
14	lnc-COMMD10-6	chr5:115661716-115661988	l_3000_chr5:115661715-115668338_thyroid
15	lnc-SEMA6A-1	chr5:115703287-115706170	ENSG00000249280
16	lnc-LVRN.1-4	chr5:115637354-115638100	NONHSAT103359
17	lnc-LVRN.1-3	chr5:115549572-115550152	NONHSAT103355
18	lnc-LVRN.1-4	chr5:115638966-115639380	NONHSAT103359
19	lnc-SEMA6A-1	chr5:115710179-115710267	NONHSAT103361
20	lnc-ATG12-5	chr5:115419214-115420722	NONHSAT103353
21	lnc-LVRN.1-4	chr5:115633944-115634089	NONHSAT103358
22	lnc-LVRN.1-4	chr5:115633944-115634089	NONHSAT103359
23	lnc-LVRN.1-4	chr5:115717975-115718151	NONHSAT103358
24	lnc-LVRN.1-4	chr5:115632111-115632653	NONHSAT103359

No data

Variant related genes	Relation type
ENSG00000185641	TF binding region
ENSG00000271918	TF binding region
ARL14EPL	TF binding region
HMGN2P27	TF binding region
COMMD10	TF binding region
ENSG00000272265	TF binding region
ENSG00000250015	TF binding region
RNU6-644P	TF binding region
ENSG00000185641	CpG island
ENSG00000271918	CpG island
ARL14EPL	CpG island
HMGN2P27	CpG island
COMMD10	CpG island
ENSG00000272265	CpG island
ENSG00000250015	CpG island
RNU6-644P	CpG island
ENSG00000145782	chromatin interactions
ENSG00000177879	chromatin interactions
ENSG00000134970	chromatin interactions
ENSG00000103145	chromatin interactions
ENSG00000131508	chromatin interactions
ENSG00000272265	chromatin interactions
ENSG00000124198	chromatin interactions
ENSG00000173812	chromatin interactions
ENSG00000145781	chromatin interactions
ENSG00000146278	chromatin interactions
ENSG00000243414	chromatin interactions
ENSG00000232916	chromatin interactions
ENSG00000271918	chromatin interactions
ENSG00000232648	chromatin interactions
ENSG00000212457	chromatin interactions
ENSG00000131652	chromatin interactions
ENSG00000271931	chromatin interactions
ENSG00000251201	chromatin interactions
USP15	miRNA target sites
ACACA	miRNA target sites
BBC3	miRNA target sites

Extended variants
information (count: 16978 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:16978 , 50 per page) page: 1 2 3 4 5 6 7 ... 340

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs148325694	chr5:115384929-115384930	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs115133310	chr5:115384935-115384936	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs576613904	chr5:115384936-115384937	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs115923938	chr5:115384939-115384940	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs186775215	chr5:115384952-115384953	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs115778558	chr5:115384957-115384958	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs567125880	chr5:115387984-115387985	Inactive region	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
8	rs578090870	chr5:115387991-115387992	Inactive region	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
9	rs147852504	chr5:115388009-115388010	Inactive region	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
10	rs111656216	chr5:115388016-115388017	Inactive region	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
11	rs2662470	chr5:115388019-115388020	Inactive region	TF binding region CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs2662471	chr5:115388022-115388023	Inactive region	TF binding region CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs556820882	chr5:115388031-115388032	Inactive region	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
14	rs540787979	chr5:115388071-115388072	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs2560698	chr5:115388091-115388092	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs529522698	chr5:115388092-115388093	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs17138730	chr5:115388103-115388104	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs531384948	chr5:115390280-115390281	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs557909900	chr5:115396894-115396895	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs7703489	chr5:115396921-115396922	Inactive region	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs552738217	chr5:115396924-115396925	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs146252063	chr5:115396936-115396937	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs568066881	chr5:115396974-115396975	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs182694051	chr5:115396985-115396986	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs17494225	chr5:115396995-115396996	Inactive region	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
26	rs78499201	chr5:115397033-115397034	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs573229400	chr5:115397049-115397050	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs7707087	chr5:115397081-115397082	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs539378790	chr5:115397102-115397103	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs552878434	chr5:115397198-115397199	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs540647247	chr5:115397203-115397204	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs573038441	chr5:115397259-115397260	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs186963221	chr5:115397372-115397373	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs555788105	chr5:115397435-115397436	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs140074349	chr5:115397456-115397457	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs143736841	chr5:115397493-115397494	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs146335033	chr5:115397499-115397500	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs115313973	chr5:115397536-115397537	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs148495271	chr5:115397577-115397578	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs13356590	chr5:115397686-115397687	Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs560518892	chr5:115397693-115397694	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs529443079	chr5:115397722-115397723	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs549321072	chr5:115397797-115397798	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs142818582	chr5:115397825-115397826	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs563732689	chr5:115397854-115397855	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs532497191	chr5:115397865-115397866	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs116365442	chr5:115397868-115397869	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs577385313	chr5:115397869-115397870	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs550141517	chr5:115397921-115397922	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs62386610	chr5:115397947-115397948	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:82)

Disease	PMID	Source
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21858162	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Lung cancer	18438408	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Squamous cell cancer	20885788	CNVD
Hepatocellular carcinoma	16750200	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17133270	CNVD
Acute myeloid leukemia	20729466	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
Colorectal cancer	16272173	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Multiple myeloma	17550852	CNVD
Ovarian cancer	21720365	CNVD
Salivary gland tumor	18059337	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Renal cell carcinoma	19377443	CNVD
Prostate cancer	16461572	CNVD
Myelofibrosis	22110671	CNVD
Sezary syndrome	18413736	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Glaucoma	21310917	CNVD
Glioblastoma multiforme	22286061	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Prostate cancer	22341455	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Ependymoma	20639864	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Schizophrenia	23813976	CNVD
Renal cell carcinoma	21215367	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:4253 , 50 per page) page: 1 2 3 4 5 6 7 ... 86

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:115397000-115398400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr5:115397600-115398000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr5:115399400-115400200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr5:115400200-115403600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr5:115403600-115403800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr5:115403600-115403800	Enhancers	Liver	Liver
7	chr5:115403600-115403800	Enhancers	Fetal Heart	heart
8	chr5:115403600-115403800	Enhancers	Fetal Lung	lung
9	chr5:115403800-115409200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr5:115405400-115419600	Weak transcription	Fetal Brain Male	brain
11	chr5:115409200-115410000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr5:115410000-115410400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr5:115410400-115410600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr5:115410600-115411400	Enhancers	Primary hematopoietic stem cells short term culture	blood
15	chr5:115410600-115419400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr5:115410800-115411000	Enhancers	Fetal Intestine Large	intestine
17	chr5:115410800-115411000	Enhancers	Fetal Intestine Small	intestine
18	chr5:115410800-115411000	Enhancers	Pancreas	Pancrea
19	chr5:115410800-115411600	Enhancers	K562	blood
20	chr5:115410800-115413200	Enhancers	Primary B cells from peripheral blood	blood
21	chr5:115411000-115411200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
22	chr5:115411000-115413200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
23	chr5:115411000-115419600	Weak transcription	Fetal Intestine Small	intestine
24	chr5:115411000-115419600	Weak transcription	Pancreas	Pancrea
25	chr5:115411200-115411600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr5:115411200-115412600	Enhancers	GM12878-XiMat	blood
27	chr5:115411400-115411600	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
28	chr5:115411400-115411600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
29	chr5:115411400-115411600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr5:115411400-115413400	Enhancers	Primary monocytes fromperipheralblood	blood
31	chr5:115411400-115419600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
32	chr5:115411600-115411800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
33	chr5:115411600-115413000	Enhancers	Primary B cells from cord blood	blood
34	chr5:115411600-115413000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr5:115411600-115413200	Enhancers	Primary hematopoietic stem cells	blood
36	chr5:115411600-115413400	Enhancers	Primary hematopoietic stem cells short term culture	blood
37	chr5:115411600-115419400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
38	chr5:115411600-115419400	Weak transcription	K562	blood
39	chr5:115411600-115419600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
40	chr5:115412000-115412400	Enhancers	Monocytes-CD14+_RO01746	blood
41	chr5:115412200-115413000	Enhancers	Primary T helper cells PMA-I stimulated	--
42	chr5:115412400-115412800	Enhancers	Primary neutrophils fromperipheralblood	blood
43	chr5:115412400-115412800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
44	chr5:115412600-115413000	Flanking Active TSS	GM12878-XiMat	blood
45	chr5:115412600-115414000	Weak transcription	Fetal Stomach	stomach
46	chr5:115412600-115415600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
47	chr5:115412600-115419600	Weak transcription	Rectal Smooth Muscle	rectum
48	chr5:115412800-115413000	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
49	chr5:115412800-115413200	Enhancers	Monocytes-CD14+_RO01746	blood
50	chr5:115412800-115419800	Weak transcription	Primary neutrophils fromperipheralblood	blood

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