Variant report

Variant	esv3372411
Chromosome Location	chr7:7220952-7223800
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:7223495-7224243	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:7221373-7222749	HepG2	liver:	n/a	n/a
3	ARID3A	chr7:7221433-7222147	K562	blood:	n/a	n/a
4	ATF1	chr7:7221332-7222295	K562	blood:	n/a	n/a
5	ATF2	chr7:7221716-7222153	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr7:7222223-7222640	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr7:7221440-7222254	GM12878	blood:	n/a	chr7:7222160-7222171
8	ATF2	chr7:7221480-7222147	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF3	chr7:7221802-7222340	K562	blood:	n/a	chr7:7222159-7222172 chr7:7222159-7222172 chr7:7222160-7222173 chr7:7222162-7222172 chr7:7222159-7222170
10	BACH1	chr7:7222361-7222687	H1-hESC	embryonic stem cell:	n/a	n/a
11	BCLAF1	chr7:7221241-7222657	GM12878	blood:	n/a	chr7:7222152-7222161 chr7:7222235-7222244 chr7:7222561-7222570 chr7:7222638-7222651
12	BCLAF1	chr7:7221245-7222765	GM12878	blood:	n/a	chr7:7222152-7222161 chr7:7222235-7222244 chr7:7222561-7222570 chr7:7222638-7222651
13	BHLHE40	chr7:7221259-7222739	K562	blood:	n/a	chr7:7222139-7222155
14	BHLHE40	chr7:7221689-7222147	A549	lung:	n/a	n/a
15	BHLHE40	chr7:7221515-7222935	HepG2	liver:	n/a	chr7:7222139-7222155
16	BHLHE40	chr7:7221341-7222796	GM12878	blood:	n/a	chr7:7222139-7222155
17	BRCA1	chr7:7221440-7222038	HepG2	liver:	n/a	n/a
18	BRCA1	chr7:7223167-7223945	Hela-S3	cervix:	n/a	n/a
19	BRCA1	chr7:7221692-7222650	Hela-S3	cervix:	n/a	n/a
20	BRCA1	chr7:7222313-7222810	HepG2	liver:	n/a	n/a
21	BRCA1	chr7:7222642-7222799	GM12878	blood:	n/a	n/a
22	CBX3	chr7:7221261-7222793	K562	blood:	n/a	n/a
23	CCNT2	chr7:7221012-7223609	K562	blood:	n/a	chr7:7223299-7223308
24	CEBPB	chr7:7221962-7222442	ECC-1	luminal epithelium:	n/a	n/a
25	CEBPB	chr7:7220691-7222625	Hela-S3	cervix:	n/a	chr7:7221154-7221167
26	CEBPB	chr7:7223476-7223652	H1-hESC	embryonic stem cell:	n/a	n/a
27	CEBPB	chr7:7221384-7222524	A549	lung:	n/a	n/a
28	CEBPB	chr7:7221350-7222378	K562	blood:	n/a	n/a
29	CEBPB	chr7:7221311-7222749	HepG2	liver:	n/a	n/a
30	CEBPB	chr7:7221506-7222248	GM12878	blood:	n/a	n/a
31	CEBPB	chr7:7220715-7222385	A549	lung:	n/a	chr7:7221154-7221167
32	CEBPB	chr7:7222040-7222314	HepG2	liver:	n/a	n/a
33	CEBPB	chr7:7223520-7223841	Hela-S3	cervix:	n/a	chr7:7223828-7223840
34	CEBPB	chr7:7220660-7222551	HepG2	liver:	n/a	chr7:7221154-7221167
35	CEBPB	chr7:7220827-7222578	K562	blood:	n/a	chr7:7221154-7221167
36	CEBPB	chr7:7221968-7222380	A549	lung:	n/a	n/a
37	CEBPB	chr7:7221026-7221626	IMR90	lung:	n/a	chr7:7221154-7221167
38	CEBPB	chr7:7222007-7222279	K562	blood:	n/a	n/a
39	CEBPB	chr7:7221977-7222375	HepG2	liver:	n/a	n/a
40	CEBPD	chr7:7221744-7222439	K562	blood:	n/a	n/a
41	CEBPD	chr7:7222827-7223013	HepG2	liver:	n/a	n/a
42	CEBPD	chr7:7221814-7222607	HepG2	liver:	n/a	n/a
43	CEBPD	chr7:7221759-7222819	HepG2	liver:	n/a	n/a
44	CHD1	chr7:7222378-7223722	H1-hESC	embryonic stem cell:	n/a	chr7:7222742-7222752 chr7:7222624-7222634 chr7:7222864-7222874 chr7:7222759-7222769
45	CHD1	chr7:7221549-7222048	H1-hESC	embryonic stem cell:	n/a	n/a
46	CHD1	chr7:7221527-7223550	GM12878	blood:	n/a	chr7:7222742-7222752 chr7:7222624-7222634 chr7:7222864-7222874 chr7:7222759-7222769
47	CHD2	chr7:7221361-7223375	GM12878	blood:	n/a	chr7:7222742-7222752 chr7:7222624-7222634 chr7:7222864-7222874 chr7:7222759-7222769
48	CHD2	chr7:7221791-7223344	Hela-S3	cervix:	n/a	chr7:7222742-7222752 chr7:7222624-7222634 chr7:7222864-7222874 chr7:7222759-7222769
49	CHD2	chr7:7223098-7223333	H1-hESC	embryonic stem cell:	n/a	n/a
50	CHD2	chr7:7221383-7222946	HepG2	liver:	n/a	chr7:7222742-7222752 chr7:7222624-7222634 chr7:7222864-7222874 chr7:7222759-7222769

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:7222197-7222247	Hela-S3	cervix:	n/a
2	chr7:7222197-7222247	Hela-S3	cervix:	n/a
3	chr7:7222973-7223023	HEEpiC	esophagus:	n/a
4	chr7:7222021-7222071	Hela-S3	cervix:	n/a
5	chr7:7222021-7222071	LNCaP	prostate:	n/a
6	chr7:7221711-7221761	PrEC	prostate:	n/a
7	chr7:7222050-7222100	HMEC	breast:	n/a
8	chr7:7222021-7222071	HUVEC	blood vessel:	n/a
9	chr7:7222197-7222247	AoSMC	blood vessel:	n/a
10	chr7:7222342-7222392	Hela-S3	cervix:	n/a
11	chr7:7221711-7221761	SAEC	small airway:	n/a
12	chr7:7221920-7221970	BE2_C	brain:	n/a
13	chr7:7222222-7222272	AoSMC	blood vessel:	n/a
14	chr7:7222060-7222110	CMK	blood:	n/a
15	chr7:7222021-7222071	SK-N-MC	brain:	n/a
16	chr7:7221920-7221970	CMK	blood:	n/a
17	chr7:7222021-7222071	HPAEpiC	pulmonary alveolar:	n/a
18	chr7:7221711-7221761	HMEC	breast:	n/a
19	chr7:7222021-7222071	HRCEpiC	kidney:	n/a
20	chr7:7221920-7221970	HEEpiC	esophagus:	n/a
21	chr7:7222342-7222392	AG10803	skin:	n/a
22	chr7:7222060-7222110	T-47D	breast:	n/a
23	chr7:7221711-7221761	AG04449	skin:	fetal
24	chr7:7222060-7222110	HCM	heart:	n/a
25	chr7:7221711-7221761	SK-N-MC	brain:	n/a
26	chr7:7222342-7222392	HMEC	breast:	n/a
27	chr7:7222222-7222272	SK-N-SH_RA	brain:	n/a
28	chr7:7222197-7222247	ProgFib	skin:	n/a
29	chr7:7222060-7222110	AG09309	skin:	n/a
30	chr7:7221711-7221761	HNPCEpiC	eye:	n/a
31	chr7:7222222-7222272	HPAEpiC	pulmonary alveolar:	n/a
32	chr7:7222973-7223023	SKMC	muscle:	n/a
33	chr7:7221920-7221970	HEK293	kidney:	embryo
34	chr7:7222973-7223023	IMR90	lung:	fetal
35	chr7:7222973-7223023	HCM	heart:	n/a
36	chr7:7222973-7223023	GM12878	blood:	n/a
37	chr7:7222342-7222392	IMR90	lung:	fetal
38	chr7:7222197-7222247	HCF	heart:	n/a
39	chr7:7222021-7222071	MCF-7	breast:	n/a
40	chr7:7222021-7222071	PANC-1	pancreas:	n/a
41	chr7:7222973-7223023	NB4	blood:	n/a
42	chr7:7222342-7222392	Jurkat	blood:	n/a
43	chr7:7222060-7222110	HRPEpiC	eye:	n/a
44	chr7:7222197-7222247	SK-N-SH	brain:	n/a
45	chr7:7221711-7221761	LNCaP	prostate:	n/a
46	chr7:7222222-7222272	Hepatocyte	liver:	n/a
47	chr7:7222050-7222100	NH-A	brain:	n/a
48	chr7:7222973-7223023	Caco-2	colon:	n/a
49	chr7:7221920-7221970	AG09309	skin:	n/a
50	chr7:7222197-7222247	SK-N-SH_RA	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr20:42087032..42087701-chr7:7221482..7222050,2	Hela-S3	cervix:
2	chr15:90776699..90777449-chr7:7221482..7222271,2	Hela-S3	cervix:
3	chr7:7220424..7222400-chr7:7606398..7608085,2	K562	blood:
4	chr7:7220051..7223731-chr7:7605300..7608795,5	K562	blood:
5	chr12:42537869..42538573-chr7:7221502..7222431,2	Hela-S3	cervix:
6	chr7:7220227..7222107-chr7:7381152..7382805,2	MCF-7	breast:
7	chr11:62608960..62609483-chr7:7221717..7222360,2	HCT-116	colon:
8	chr7:7223378..7225133-chr7:7233745..7235333,2	K562	blood:
9	chr7:7221023..7222531-chr7:7605504..7608100,2	MCF-7	breast:
10	chr7:7138712..7144572-chr7:7219459..7223789,7	K562	blood:
11	chr7:7221414..7222034-chr7:30544206..30545163,2	NB4	blood:
12	chr1:16678905..16679436-chr7:7221264..7221969,2	HCT-116	colon:
13	chr1:151253957..151254628-chr7:7222523..7223125,2	Hela-S3	cervix:
14	chr15:74753446..74754078-chr7:7222511..7223403,2	Hela-S3	cervix:
15	chr17:73775419..73776051-chr7:7222174..7223063,2	Hela-S3	cervix:
16	chr7:7213763..7219997-chr7:7220116..7223880,12	MCF-7	breast:
17	chr17:56708791..56709544-chr7:7222232..7223001,2	Hela-S3	cervix:
18	chr3:10183327..10184184-chr7:7221819..7222735,2	Hela-S3	cervix:
19	chr3:41240799..41241491-chr7:7221499..7222498,2	Hela-S3	cervix:
20	chr16:2014763..2015531-chr7:7222810..7223779,2	Hela-S3	cervix:
21	chr7:7138294..7142693-chr7:7219176..7223789,9	K562	blood:
22	chr13:108870463..108871035-chr7:7221964..7222642,2	HCT-116	colon:
23	chr2:211034902..211035782-chr7:7221578..7222378,2	NB4	blood:

Variant related genes	Relation type
C1GALT1	TF binding region
C1GALT1	CpG island
ENSG00000168036	chromatin interactions
ENSG00000132475	chromatin interactions
ENSG00000174405	chromatin interactions
ENSG00000247240	chromatin interactions
ENSG00000144445	chromatin interactions
ENSG00000140988	chromatin interactions
ENSG00000143373	chromatin interactions
ENSG00000164654	chromatin interactions
ENSG00000212195	chromatin interactions
ENSG00000232671	chromatin interactions
ENSG00000151233	chromatin interactions
ENSG00000185043	chromatin interactions
ENSG00000138629	chromatin interactions
ENSG00000139826	chromatin interactions
ENSG00000006625	chromatin interactions
ENSG00000255198	chromatin interactions
ENSG00000201218	chromatin interactions
ENSG00000244167	chromatin interactions
ENSG00000055070	chromatin interactions
ENSG00000183208	chromatin interactions
ENSG00000272894	chromatin interactions
ENSG00000037637	chromatin interactions
ENSG00000134086	chromatin interactions
ENSG00000133316	chromatin interactions

Extended variants
information (count: 135 )
Associated
traits (count: 76 )

Variant overlapped rSNPs/rCNVs (count:135 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs569234141	chr7:7220964-7220965	Flanking Active TSS Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
2	rs536649851	chr7:7220993-7220994	Flanking Active TSS Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
3	rs555047580	chr7:7221098-7221099	Flanking Active TSS Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
4	rs74324416	chr7:7221120-7221121	Flanking Active TSS Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
5	rs186045457	chr7:7221178-7221179	Flanking Active TSS Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
6	rs537780183	chr7:7221192-7221193	Flanking Active TSS Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
7	rs556412790	chr7:7221237-7221238	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
8	rs558864631	chr7:7221318-7221319	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
9	rs577390958	chr7:7221320-7221321	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
10	rs34983897	chr7:7221380-7221381	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
11	rs544545415	chr7:7221387-7221388	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
12	rs556827990	chr7:7221402-7221403	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
13	rs574051153	chr7:7221418-7221419	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
14	rs740534	chr7:7221427-7221428	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs559759839	chr7:7221471-7221472	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
16	rs76453007	chr7:7221505-7221506	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
17	rs80147803	chr7:7221538-7221539	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
18	rs564089720	chr7:7221549-7221550	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
19	rs531539783	chr7:7221573-7221574	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
20	rs740533	chr7:7221577-7221578	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	12 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs141741043	chr7:7221586-7221587	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
22	rs191292674	chr7:7221592-7221593	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
23	rs183039039	chr7:7221610-7221611	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
24	rs572077002	chr7:7221668-7221669	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
25	rs7803202	chr7:7221673-7221674	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	13 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs534009921	chr7:7221691-7221692	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
27	rs55801576	chr7:7221693-7221694	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
28	rs559026575	chr7:7221703-7221704	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
29	rs570917131	chr7:7221718-7221719	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
30	rs147184446	chr7:7221721-7221722	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
31	rs138953333	chr7:7221728-7221729	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
32	rs550847621	chr7:7221738-7221739	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
33	rs185904653	chr7:7221770-7221771	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
34	rs7803355	chr7:7221775-7221776	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	14 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
35	rs544963854	chr7:7221824-7221825	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
36	rs553321632	chr7:7221837-7221838	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
37	rs142925107	chr7:7221838-7221839	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
38	rs557517738	chr7:7221863-7221864	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
39	rs114307654	chr7:7221878-7221879	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
40	rs564211328	chr7:7221899-7221900	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
41	rs373094065	chr7:7221905-7221906	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
42	rs13229375	chr7:7221907-7221908	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	15 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs7803534	chr7:7221924-7221925	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	15 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs529182192	chr7:7221937-7221938	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
45	rs13243458	chr7:7221952-7221953	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	15 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs758263	chr7:7221968-7221969	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	17 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
47	rs527694559	chr7:7221981-7221982	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
48	rs740532	chr7:7221982-7221983	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	15 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs570924031	chr7:7221991-7221992	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
50	rs537997544	chr7:7221997-7221998	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:76)

Disease	PMID	Source
Sudden cardiac death	19188705	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Glioma	18556773	CNVD
Ovarian cancer	21720365	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Ovarian cancer	22174824	CNVD
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
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
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Acute myeloid leukemia	21251322	CNVD
Glioblastoma multiforme	21525872	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Melanoma	17363583	CNVD
Lung adenocarcinoma	21935476	CNVD
Ovarian cancer	21781307	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16272173	CNVD
Hirschsprung''s Disease	21712996	CNVD
Glioblastoma multiforme	22286061	CNVD
Non-small cell lung cancer	21829676	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Kartagener syndrome	16639409	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD

Chromatin state (count:439 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:7216800-7221000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
2	chr7:7216800-7221200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
3	chr7:7217000-7221000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr7:7217000-7221000	Weak transcription	Cortex derived primary cultured neurospheres	brain
5	chr7:7217200-7221200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
6	chr7:7217600-7221000	Weak transcription	NH-A	brain
7	chr7:7217800-7221200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr7:7218800-7221000	Weak transcription	Placenta Amnion	Placenta Amnion
9	chr7:7220200-7221000	Enhancers	iPS-20b Cell Line	embryonic stem cell
10	chr7:7220400-7221000	Enhancers	iPS-18 Cell Line	embryonic stem cell
11	chr7:7220400-7221000	Enhancers	Primary T cells fromperipheralblood	blood
12	chr7:7220400-7221000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
13	chr7:7220400-7221000	Enhancers	HSMM	muscle
14	chr7:7220400-7221200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr7:7220400-7221200	Enhancers	H9 Cell Line	embryonic stem cell
16	chr7:7220400-7221200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
17	chr7:7220400-7221200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr7:7220400-7221200	Enhancers	Primary B cells from peripheral blood	blood
19	chr7:7220400-7221200	Enhancers	Pancreas	Pancrea
20	chr7:7220400-7221400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr7:7220400-7221600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
22	chr7:7220600-7221000	Enhancers	HUES64 Cell Line	embryonic stem cell
23	chr7:7220600-7221000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
24	chr7:7220600-7221400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
25	chr7:7220600-7221800	Flanking Active TSS	Primary B cells from cord blood	blood
26	chr7:7220600-7224000	Active TSS	Rectal Mucosa Donor 29	rectum
27	chr7:7220800-7221000	Flanking Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr7:7220800-7221000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
29	chr7:7220800-7221000	Enhancers	Breast Myoepithelial Primary Cells	Breast
30	chr7:7220800-7221000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
31	chr7:7220800-7221000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
32	chr7:7220800-7221000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
33	chr7:7220800-7221000	Enhancers	Primary T regulatory cells fromperipheralblood	blood
34	chr7:7220800-7221000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
35	chr7:7220800-7221000	Enhancers	Primary T killer memory cells from peripheral blood	blood
36	chr7:7220800-7221000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
37	chr7:7220800-7221000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
38	chr7:7220800-7221000	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
39	chr7:7220800-7221000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
40	chr7:7220800-7221000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr7:7220800-7221000	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
42	chr7:7220800-7221000	Enhancers	Adipose Nuclei	Adipose
43	chr7:7220800-7221000	Enhancers	Brain Hippocampus Middle	brain
44	chr7:7220800-7221000	Active TSS	Brain Inferior Temporal Lobe	brain
45	chr7:7220800-7221000	Enhancers	Brain Substantia Nigra	brain
46	chr7:7220800-7221000	Enhancers	Duodenum Smooth Muscle	Duodenum
47	chr7:7220800-7221000	Flanking Active TSS	Fetal Kidney	kidney
48	chr7:7220800-7221000	Enhancers	Pancreatic Islets	Pancreatic Islet
49	chr7:7220800-7221000	Enhancers	Fetal Stomach	stomach
50	chr7:7220800-7221000	Enhancers	Fetal Thymus	thymus

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