Variant report

Variant	nsv576482
Chromosome Location	chr18:11362587-11557161
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1959)
CpG islands
(count:61)
Chromatin interactive
region (count:26)
LncRNA
region (count:88)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1959 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr18:11500265-11501942	HepG2	liver:	n/a	n/a
2	ARID3A	chr18:11512685-11512993	HepG2	liver:	n/a	n/a
3	ARID3A	chr18:11497589-11497898	HepG2	liver:	n/a	n/a
4	ARID3A	chr18:11519203-11519408	HepG2	liver:	n/a	n/a
5	ARID3A	chr18:11493958-11494614	HepG2	liver:	n/a	chr18:11494545-11494561
6	ATF2	chr18:11511325-11511711	GM12878	blood:	n/a	n/a
7	ATF2	chr18:11511354-11511912	GM12878	blood:	n/a	n/a
8	ATF3	chr18:11519178-11519339	K562	blood:	n/a	n/a
9	ATF3	chr18:11519029-11519344	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr18:11388405-11388414	K562	blood:	n/a	n/a
11	BACH1	chr18:11468208-11468461	H1-hESC	embryonic stem cell:	n/a	n/a
12	BATF	chr18:11500458-11500756	GM12878	blood:	n/a	n/a
13	BATF	chr18:11367943-11368357	GM12878	blood:	n/a	n/a
14	BATF	chr18:11387929-11388160	GM12878	blood:	n/a	n/a
15	BATF	chr18:11367921-11368318	GM12878	blood:	n/a	n/a
16	BATF	chr18:11437092-11437379	GM12878	blood:	n/a	n/a
17	BCL11A	chr18:11367995-11368321	GM12878	blood:	n/a	n/a
18	BCL11A	chr18:11367993-11368334	GM12878	blood:	n/a	n/a
19	BCLAF1	chr18:11419356-11419720	GM12878	blood:	n/a	n/a
20	BHLHE40	chr18:11511453-11512073	GM12878	blood:	n/a	n/a
21	BHLHE40	chr18:11391796-11391825	K562	blood:	n/a	n/a
22	BHLHE40	chr18:11533514-11533708	K562	blood:	n/a	n/a
23	BHLHE40	chr18:11500447-11501074	HepG2	liver:	n/a	n/a
24	BHLHE40	chr18:11519095-11519341	K562	blood:	n/a	n/a
25	BHLHE40	chr18:11553397-11553707	GM12878	blood:	n/a	n/a
26	BHLHE40	chr18:11405971-11406112	K562	blood:	n/a	chr18:11405985-11406006 chr18:11405992-11406001 chr18:11405989-11406002 chr18:11405991-11406000 chr18:11405991-11406000 chr18:11405990-11405999
27	BHLHE40	chr18:11532341-11532541	HepG2	liver:	n/a	n/a
28	BRCA1	chr18:11500467-11500505	HepG2	liver:	n/a	n/a
29	BRCA1	chr18:11553368-11553604	Hela-S3	cervix:	n/a	n/a
30	BRCA1	chr18:11519100-11519333	H1-hESC	embryonic stem cell:	n/a	n/a
31	BRCA1	chr18:11488272-11488735	Hela-S3	cervix:	n/a	n/a
32	BRCA1	chr18:11496621-11496902	Hela-S3	cervix:	n/a	n/a
33	BRCA1	chr18:11388046-11388227	HepG2	liver:	n/a	n/a
34	BRCA1	chr18:11500423-11500877	Hela-S3	cervix:	n/a	n/a
35	BRCA1	chr18:11506874-11507253	Hela-S3	cervix:	n/a	n/a
36	BRCA1	chr18:11464371-11464386	HepG2	liver:	n/a	n/a
37	BRCA1	chr18:11366509-11366746	Hela-S3	cervix:	n/a	n/a
38	CBX3	chr18:11544142-11544394	K562	blood:	n/a	n/a
39	CBX3	chr18:11500325-11500942	HCT-116	colon:	n/a	n/a
40	CBX3	chr18:11544117-11544406	K562	blood:	n/a	n/a
41	CBX3	chr18:11500362-11500760	HCT-116	colon:	n/a	n/a
42	CBX3	chr18:11544082-11544485	HCT-116	colon:	n/a	n/a
43	CBX3	chr18:11544140-11544504	HCT-116	colon:	n/a	n/a
44	CEBPB	chr18:11445492-11445590	A549	lung:	n/a	n/a
45	CEBPB	chr18:11437127-11437307	H1-hESC	embryonic stem cell:	n/a	n/a
46	CEBPB	chr18:11496452-11496922	Hela-S3	cervix:	n/a	n/a
47	CEBPB	chr18:11519104-11519317	HepG2	liver:	n/a	n/a
48	CEBPB	chr18:11431880-11432174	K562	blood:	n/a	n/a
49	CEBPB	chr18:11496592-11496916	MCF-7	breast:	n/a	n/a
50	CEBPB	chr18:11407918-11408230	IMR90	lung:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr18:11519034-11519084	GM12878	blood:	n/a
2	chr18:11519034-11519084	MCF10A-Er-Src	breast:	n/a
3	chr18:11519034-11519084	NB4	blood:	n/a
4	chr18:11519034-11519084	AoSMC	blood vessel:	n/a
5	chr18:11519034-11519084	HMEC	breast:	n/a
6	chr18:11519034-11519084	NH-A	brain:	n/a
7	chr18:11519034-11519084	Caco-2	colon:	n/a
8	chr18:11519034-11519084	BJ	skin:	n/a
9	chr18:11519034-11519084	ovcar-3	ovarian:	n/a
10	chr18:11519034-11519084	RPTEC	kidney:	n/a
11	chr18:11519034-11519084	HUVEC	blood vessel:	n/a
12	chr18:11519034-11519084	HRCEpiC	kidney:	n/a
13	chr18:11519034-11519084	SK-N-SH	brain:	n/a
14	chr18:11519034-11519084	PANC-1	pancreas:	n/a
15	chr18:11519034-11519084	SAEC	small airway:	n/a
16	chr18:11519034-11519084	AG09319	gingival:	n/a
17	chr18:11519034-11519084	CMK	blood:	n/a
18	chr18:11519034-11519084	HL-60	blood:	n/a
19	chr18:11519034-11519084	K562	blood:	n/a
20	chr18:11519034-11519084	AG04450	lung:	fetal
21	chr18:11519034-11519084	U87	brain:	n/a
22	chr18:11519034-11519084	HNPCEpiC	eye:	n/a
23	chr18:11519034-11519084	HAEpiC	amniotic membrane:	n/a
24	chr18:11519034-11519084	ProgFib	skin:	n/a
25	chr18:11519034-11519084	GM06990	blood:	n/a
26	chr18:11519034-11519084	AG04449	skin:	fetal
27	chr18:11519034-11519084	PrEC	prostate:	n/a
28	chr18:11519034-11519084	Hela-S3	cervix:	n/a
29	chr18:11519034-11519084	NT2-D1	testis:	n/a
30	chr18:11519034-11519084	NHBE	bronchial:	n/a
31	chr18:11519034-11519084	HRPEpiC	eye:	n/a
32	chr18:11519034-11519084	H1-hESC	embryonic stem cell:	embryo
33	chr18:11519034-11519084	T-47D	breast:	n/a
34	chr18:11519034-11519084	SK-N-MC	brain:	n/a
35	chr18:11519034-11519084	HRE	kidney:	n/a
36	chr18:11519034-11519084	HCM	heart:	n/a
37	chr18:11519034-11519084	HCPEpiC	choroid plexus:	n/a
38	chr18:11519034-11519084	HCF	heart:	n/a
39	chr18:11519034-11519084	AG09309	skin:	n/a
40	chr18:11519034-11519084	ECC-1	luminal epithelium:	n/a
41	chr18:11519034-11519084	GM19239	blood:	n/a
42	chr18:11519034-11519084	BE2_C	brain:	n/a
43	chr18:11519034-11519084	GM12891	blood:	n/a
44	chr18:11519034-11519084	PFSK-1	brain:	n/a
45	chr18:11519034-11519084	Hepatocyte	liver:	n/a
46	chr18:11519034-11519084	A549	lung:	n/a
47	chr18:11519034-11519084	GM12892	blood:	n/a
48	chr18:11519034-11519084	SK-N-SH_RA	brain:	n/a
49	chr18:11519034-11519084	HPAEpiC	pulmonary alveolar:	n/a
50	chr18:11519034-11519084	HEEpiC	esophagus:	n/a

(count:26 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:151965186..151965687-chr18:11365448..11365948,2	Hela-S3	cervix:
2	chr18:11494387..11496981-chr18:11498491..11500808,2	MCF-7	breast:
3	chr18:11387860..11389856-chr18:11391492..11394424,2	MCF-7	breast:
4	chr18:11310565..11311185-chr18:11413212..11414156,2	K562	blood:
5	chr18:11365422..11368107-chr18:11369028..11370592,2	K562	blood:
6	chr18:11454276..11456483-chr18:11456790..11459275,2	MCF-7	breast:
7	chr18:11487890..11489890-chr18:11494486..11496353,2	K562	blood:
8	chr18:11518713..11519703-chr18:11552996..11553743,6	MCF-7	breast:
9	chr18:11513286..11515221-chr18:11517194..11519674,2	K562	blood:
10	chr18:11310495..11311249-chr18:11553049..11553579,2	MCF-7	breast:
11	chr18:11440473..11443094-chr18:11444494..11446221,2	K562	blood:
12	chr18:11310235..11310873-chr18:11387558..11388316,3	MCF-7	breast:
13	chr18:11518909..11519601-chr18:11549107..11549874,2	MCF-7	breast:
14	chr18:11365422..11368107-chr18:11369028..11370592,2	K562	blood:
15	chr18:11513286..11515221-chr18:11517194..11519674,2	K562	blood:
16	chr18:11268822..11269508-chr18:11500370..11501110,2	MCF-7	breast:
17	chr18:11484260..11486472-chr18:11488941..11490761,2	MCF-7	breast:
18	chr18:11440473..11443094-chr18:11444494..11446221,2	K562	blood:
19	chr18:11387860..11389856-chr18:11391492..11394424,2	MCF-7	breast:
20	chr18:11464572..11467266-chr18:11469004..11470524,2	K562	blood:
21	chr18:11487890..11489675-chr18:11493773..11495986,2	K562	blood:
22	chr18:11518713..11519703-chr18:11552996..11553743,6	MCF-7	breast:
23	chr18:11309816..11310769-chr18:11512438..11513268,3	MCF-7	breast:
24	chr18:11464572..11467266-chr18:11469004..11470524,2	K562	blood:
25	chr18:11518909..11519601-chr18:11549107..11549874,2	MCF-7	breast:
26	chr18:11494387..11496981-chr18:11498491..11500808,2	MCF-7	breast:

(count:88 , 50 per page) page: 1 2

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PIEZO2-3	chr18:11410813-11410947	NONHSAT057297
2	lnc-SLC35G4-1	chr18:11490223-11490240	ENSG00000267252.1
3	lnc-PIEZO2-3	chr18:11368532-11368651	NONHSAT057297
4	lnc-SLC35G4-1	chr18:11506756-11506979	XLOC_012626
5	lnc-SLC35G4-1	chr18:11490029-11490240	XLOC_012626
6	lnc-SLC35G4-1	chr18:11488833-11488921	ENSG00000267252.1
7	lnc-SLC35G4-5	chr18:11478833-11478921	l_1527_chr18:11477425-11478921_testes
8	lnc-PIEZO2-3	chr18:11376001-11376371	XLOC_012768
9	lnc-SLC35G4-1	chr18:11488989-11490240	NONHSAT057308
10	lnc-SLC35G4-6	chr18:11454477-11454532	ENSG00000267425.1
11	lnc-SLC35G4-6	chr18:11465276-11465509	NONHSAT057303
12	lnc-SLC35G4-1	chr18:11505503-11506635	XLOC_012626
13	lnc-SLC35G4-1	chr18:11506755-11506982	NONHSAT057314
14	lnc-SLC35G4-4	chr18:11480379-11480950	l_1528_chr18:11480028-11481803_testes
15	lnc-RP11-677O4.1.1-2	chr18:11447748-11447989	XLOC_012769
16	lnc-SLC35G4-4	chr18:11494700-11495230	l_1528_chr18:11480028-11481803_testes
17	lnc-SLC35G4-1	chr18:11503733-11503883	ENSG00000267252.1
18	lnc-RP11-677O4.1.1-3	chr18:11461253-11461279	l_1526_chr18:11437747-11480012_testes
19	lnc-SLC35G4-1	chr18:11490769-11490964	ENSG00000267252.1
20	lnc-PIEZO2-3	chr18:11368532-11368651	ENSG00000267051.1
21	lnc-PIEZO2-3	chr18:11367164-11367446	NONHSAT057297
22	lnc-RP11-677O4.1.1-2	chr18:11490466-11490670	XLOC_012769
23	lnc-SLC35G4-6	chr18:11465276-11465509	ENSG00000267425.1
24	lnc-SLC35G4-1	chr18:11490379-11490892	ENSG00000267252.1
25	lnc-SLC35G4-6	chr18:11454055-11454532	NONHSAT057303
26	lnc-SLC35G4-1	chr18:11506756-11506975	ENSG00000267252.1
27	lnc-RP11-677O4.1.1-2	chr18:11489325-11489882	NONHSAT057304
28	lnc-PIEZO2-11	chr18:11368259-11368392	l_1525_chr18:11356975-11368345_testes
29	lnc-SLC35G4-1	chr18:11506531-11506635	ENSG00000267252.1
30	lnc-RP11-677O4.1.1-3	chr18:11437748-11437989	l_1526_chr18:11437747-11480012_testes
31	lnc-SLC35G4-4	chr18:11495257-11496635	l_1528_chr18:11480028-11481803_testes
32	lnc-SLC35G4-1	chr18:11487834-11488594	XLOC_012626
33	lnc-RP11-677O4.1.1-3	chr18:11479325-11480012	l_1526_chr18:11437747-11480012_testes
34	lnc-SLC35G4-6	chr18:11465869-11466469	NONHSAT057303
35	lnc-PIEZO2-3	chr18:11378261-11378345	XLOC_012768
36	lnc-SLC35G4-1	chr18:11488833-11488921	XLOC_012626
37	lnc-SLC35G4-1	chr18:11490047-11490240	ENSG00000267252.1
38	lnc-SLC35G4-1	chr18:11506756-11506967	ENSG00000267252.1
39	lnc-SLC35G4-1	chr18:11506531-11506635	XLOC_012626
40	lnc-RP11-677O4.1.1-4	chr18:11390032-11390728	ENSG00000273119.1
41	lnc-PIEZO2-3	chr18:11368532-11368644	XLOC_012768
42	lnc-SLC35G4-1	chr18:11506531-11506635	XLOC_012626
43	lnc-SLC35G4-1	chr18:11490029-11490240	XLOC_012626
44	lnc-SLC35G4-4	chr18:11480979-11481803	l_1528_chr18:11480028-11481803_testes
45	lnc-PIEZO2-3	chr18:11366912-11367446	ENSG00000267051.1
46	lnc-SLC35G4-1	chr18:11506531-11506635	ENSG00000267252.1
47	lnc-RP11-677O4.1.1-2	chr18:11447608-11447989	XLOC_012769
48	lnc-SLC35G4-1	chr18:11503733-11503935	XLOC_012626
49	lnc-SLC35G4-1	chr18:11487994-11488594	XLOC_012626
50	lnc-SLC35G4-1	chr18:11506531-11506635	NONHSAT057308

No data

Variant related genes	Relation type
ENSG00000267252	TF binding region
ENSG00000267425	TF binding region
ENSG00000267051	TF binding region
ENSG00000267371	TF binding region
ENSG00000273119	TF binding region
ENSG00000267564	TF binding region
ENSG00000267252	CpG island
ENSG00000267425	CpG island
ENSG00000267051	CpG island
ENSG00000267371	CpG island
ENSG00000273119	CpG island
ENSG00000267564	CpG island
ENSG00000267252	chromatin interactions
ENSG00000267425	chromatin interactions
ENSG00000267564	chromatin interactions
SLC30A7	miRNA target sites
EPB41	miRNA target sites
TMEM9B	miRNA target sites
BICD2	miRNA target sites
TGFBR2	miRNA target sites
TMF1	miRNA target sites
CLCN3	miRNA target sites
NUP153	miRNA target sites
SLC30A6	miRNA target sites

Extended variants
information (count: 6370 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:6370 , 50 per page) page: 1 2 3 4 5 6 7 ... 128

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4797529	chr18:11362587-11362588	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs147306704	chr18:11362625-11362626	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs535752070	chr18:11362727-11362728	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs543483800	chr18:11362729-11362730	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs74361553	chr18:11362786-11362787	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs375770587	chr18:11362795-11362796	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs139549057	chr18:11362808-11362809	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs559594274	chr18:11362810-11362811	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs572221188	chr18:11362821-11362822	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs188064966	chr18:11362856-11362857	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs145088814	chr18:11362914-11362915	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs147589285	chr18:11362942-11362943	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs567646718	chr18:11362956-11362957	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs74483797	chr18:11363012-11363013	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs549845551	chr18:11363020-11363021	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs191426156	chr18:11363081-11363082	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs182407813	chr18:11363109-11363110	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs116536570	chr18:11363128-11363129	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs534626591	chr18:11363139-11363140	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs564383438	chr18:11363172-11363173	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs78274903	chr18:11363180-11363181	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs372935767	chr18:11363209-11363210	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs575976613	chr18:11363248-11363249	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs543016782	chr18:11363253-11363254	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs558609981	chr18:11363272-11363273	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs576968595	chr18:11363313-11363314	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs531553333	chr18:11363321-11363322	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs541139097	chr18:11363330-11363331	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs559581007	chr18:11363378-11363379	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs550341240	chr18:11363422-11363423	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs550187567	chr18:11363423-11363424	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs529892512	chr18:11363434-11363435	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs542084383	chr18:11363452-11363453	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs151217309	chr18:11363481-11363482	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs188208220	chr18:11363491-11363492	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs549736590	chr18:11363553-11363554	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs541052482	chr18:11363667-11363668	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs562072890	chr18:11363672-11363673	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs192739208	chr18:11363702-11363703	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs532427430	chr18:11363704-11363705	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs185173983	chr18:11363791-11363792	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs375937203	chr18:11363797-11363798	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs566243459	chr18:11363798-11363799	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs201355788	chr18:11363822-11363823	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs368114286	chr18:11363824-11363825	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs200783077	chr18:11363825-11363826	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs35122739	chr18:11363841-11363842	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs562179601	chr18:11363888-11363889	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs140406536	chr18:11363889-11363890	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs555160565	chr18:11363905-11363906	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:61)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Intellectual disability	22102821	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Acute myeloid leukemia	16864856	CNVD
Seminomas	18059402	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Kartagener syndrome	16639409	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Cancer	21183584	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Human rectal carcinomas	16397240	CNVD
Melanoma	18172304	CNVD
Colorectal cancer	16272173	CNVD
Colorectal cancer	19150955	CNVD
Follicular lymphoma	20505157	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	18923191	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	21637783	CNVD
Medulloblastoma	21979893	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Trisomy 18 syndrome	17576883	CNVD
Breast cancer	21785460	CNVD
Autism	20808228	CNVD
lymphocytic leukemia	21291569	CNVD
Barrett''s syndrome	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Ewing''s sarcoma	17952124	CNVD
Multiple myeloma	17550852	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21858162	CNVD
small cell lung cancer	20016488	CNVD
abnormal development	18461090	CNVD
Heart disease	21282601	CNVD
Glioblastoma multiforme	21922591	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute myeloid leukemia	17377590	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Developmental delay	21147756	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16620391	CNVD
Myelofibrosis	22110671	CNVD
Retinoblastoma	21504564	CNVD
Glioma	17123091	CNVD
Neurodevelopmental disorder	22521361	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:562 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:11361200-11364400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr18:11364400-11369400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr18:11364800-11365000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr18:11365000-11366000	Weak transcription	Skeletal Muscle Female	skeletal muscle
5	chr18:11365200-11366400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
6	chr18:11366000-11366200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr18:11366000-11366200	Enhancers	Skeletal Muscle Female	skeletal muscle
8	chr18:11366000-11366400	Enhancers	HSMMtube	muscle
9	chr18:11366000-11367400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
10	chr18:11366000-11367800	Enhancers	Fetal Heart	heart
11	chr18:11366000-11367800	Enhancers	Skeletal Muscle Male	skeletal muscle
12	chr18:11366200-11366400	Enhancers	Muscle Satellite Cultured Cells	--
13	chr18:11366200-11366400	Enhancers	Osteobl	bone
14	chr18:11366200-11366600	Active TSS	Skeletal Muscle Female	skeletal muscle
15	chr18:11366200-11367000	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
16	chr18:11366200-11367200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
17	chr18:11366200-11368200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr18:11366200-11368600	Enhancers	HSMM	muscle
19	chr18:11366400-11366800	Enhancers	HUES6 Cell Line	embryonic stem cell
20	chr18:11366400-11366800	Enhancers	Cortex derived primary cultured neurospheres	brain
21	chr18:11366400-11366800	Enhancers	NH-A	brain
22	chr18:11366400-11366800	Enhancers	NHLF	lung
23	chr18:11366400-11366800	Flanking Active TSS	Osteobl	bone
24	chr18:11366400-11367000	Enhancers	ES-I3 Cell Line	embryonic stem cell
25	chr18:11366400-11367000	Enhancers	HUES64 Cell Line	embryonic stem cell
26	chr18:11366400-11367000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
27	chr18:11366400-11367000	Flanking Active TSS	HSMMtube	muscle
28	chr18:11366400-11367400	Flanking Active TSS	Muscle Satellite Cultured Cells	--
29	chr18:11366400-11367400	Enhancers	Hela-S3	cervix
30	chr18:11366400-11367600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr18:11366400-11367600	Enhancers	Fetal Muscle Leg	muscle
32	chr18:11366400-11367800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
33	chr18:11366400-11368400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
34	chr18:11366400-11368800	Enhancers	NHDF-Ad	bronchial
35	chr18:11366600-11368000	Enhancers	Psoas Muscle	Psoas
36	chr18:11366600-11368200	Enhancers	Skeletal Muscle Female	skeletal muscle
37	chr18:11366800-11367200	Enhancers	Brain Cingulate Gyrus	brain
38	chr18:11366800-11367600	Enhancers	Osteobl	bone
39	chr18:11367000-11367400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
40	chr18:11367000-11367600	Enhancers	HSMMtube	muscle
41	chr18:11367000-11368200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
42	chr18:11367400-11368800	Enhancers	Muscle Satellite Cultured Cells	--
43	chr18:11367600-11368000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr18:11367600-11368200	Weak transcription	Osteobl	bone
45	chr18:11367600-11383600	Weak transcription	Fetal Muscle Leg	muscle
46	chr18:11367800-11374000	Weak transcription	Skeletal Muscle Male	skeletal muscle
47	chr18:11367800-11377400	Weak transcription	Fetal Heart	heart
48	chr18:11368000-11368400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr18:11368200-11368400	Enhancers	Osteobl	bone
50	chr18:11368600-11370000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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