Variant report

Variant	nsv5629
Chromosome Location	chr7:6217866-6263131
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:288)
CpG islands
(count:183)
Chromatin interactive
region (count:23)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:288 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:6260839-6261320	K562	blood:	n/a	n/a
2	ATF1	chr7:6260898-6261370	K562	blood:	n/a	n/a
3	ATF2	chr7:6260931-6261248	GM12878	blood:	n/a	n/a
4	ATF2	chr7:6220717-6221092	GM12878	blood:	n/a	n/a
5	ATF2	chr7:6220664-6221194	GM12878	blood:	n/a	n/a
6	ATF3	chr7:6260900-6261277	K562	blood:	n/a	n/a
7	BACH1	chr7:6242971-6243339	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr7:6251663-6252024	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr7:6251715-6251969	K562	blood:	n/a	n/a
10	BACH1	chr7:6243063-6243241	K562	blood:	n/a	n/a
11	BATF	chr7:6260932-6261318	GM12878	blood:	n/a	n/a
12	BATF	chr7:6220796-6221092	GM12878	blood:	n/a	n/a
13	BATF	chr7:6261031-6261247	GM12878	blood:	n/a	n/a
14	BHLHE40	chr7:6248948-6249313	K562	blood:	n/a	chr7:6249142-6249151 chr7:6249135-6249156
15	BHLHE40	chr7:6260956-6261235	K562	blood:	n/a	n/a
16	BHLHE40	chr7:6251782-6251965	K562	blood:	n/a	n/a
17	CCNT2	chr7:6260913-6261287	K562	blood:	n/a	n/a
18	CEBPB	chr7:6260961-6261409	MCF-7	breast:	n/a	n/a
19	CEBPB	chr7:6261003-6261414	K562	blood:	n/a	n/a
20	CEBPB	chr7:6261011-6261278	K562	blood:	n/a	n/a
21	CEBPB	chr7:6260954-6261482	A549	lung:	n/a	n/a
22	CEBPB	chr7:6220898-6221015	A549	lung:	n/a	chr7:6220945-6220954 chr7:6220945-6220956
23	CEBPB	chr7:6258969-6259202	Hela-S3	cervix:	n/a	n/a
24	CEBPB	chr7:6261000-6261393	IMR90	lung:	n/a	n/a
25	CEBPB	chr7:6224118-6224371	MCF-7	breast:	n/a	chr7:6224267-6224278
26	CEBPB	chr7:6261042-6261431	A549	lung:	n/a	n/a
27	CEBPB	chr7:6224127-6224325	H1-hESC	embryonic stem cell:	n/a	chr7:6224267-6224278
28	CEBPB	chr7:6224217-6224299	Hela-S3	cervix:	n/a	chr7:6224267-6224278
29	CEBPB	chr7:6224196-6224383	K562	blood:	n/a	chr7:6224267-6224278
30	CEBPB	chr7:6260873-6261364	K562	blood:	n/a	n/a
31	CEBPB	chr7:6220823-6221039	K562	blood:	n/a	chr7:6220945-6220954 chr7:6220945-6220956
32	CEBPB	chr7:6224177-6224420	HepG2	liver:	n/a	chr7:6224267-6224278
33	CEBPB	chr7:6220928-6221004	Hela-S3	cervix:	n/a	chr7:6220945-6220954 chr7:6220945-6220956
34	CEBPB	chr7:6260943-6261399	Hela-S3	cervix:	n/a	n/a
35	CEBPD	chr7:6260855-6261348	K562	blood:	n/a	n/a
36	CEBPD	chr7:6260866-6261340	K562	blood:	n/a	n/a
37	CREB1	chr7:6260954-6261477	GM12878	blood:	n/a	n/a
38	CREB1	chr7:6260801-6261493	K562	blood:	n/a	n/a
39	CREB1	chr7:6260843-6261524	GM12878	blood:	n/a	n/a
40	CTCF	chr7:6226500-6226650	HEK293	kidney:	n/a	n/a
41	CTCF	chr7:6219405-6219578	GM19239	blood:	n/a	n/a
42	CTCF	chr7:6227763-6227849	Kidney_OC	kidney:	n/a	n/a
43	CTCF	chr7:6258040-6258190	AG09319	gingival:	n/a	n/a
44	CTCF	chr7:6219239-6219309	GM19239	blood:	n/a	n/a
45	CTCF	chr7:6226520-6226670	HMF	breast:	n/a	n/a
46	CTCF	chr7:6261892-6261977	Lung_OC	lung:	n/a	n/a
47	CTCF	chr7:6259122-6259138	GM20000	blood:	n/a	n/a
48	CTCF	chr7:6240471-6240543	Fibrobl	skin:	n/a	n/a
49	CTCF	chr7:6257980-6258130	AoAF	blood vessel:	n/a	n/a
50	CTCF	chr7:6219408-6219483	MCF-7	breast:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:6248449-6248499	BE2_C	brain:	n/a
2	chr7:6238486-6238536	HCT-116	colon:	n/a
3	chr7:6218888-6218938	Jurkat	blood:	n/a
4	chr7:6218888-6218938	MCF-7	breast:	n/a
5	chr7:6218888-6218938	HMEC	breast:	n/a
6	chr7:6218888-6218938	NHDF-neo	bronchial:	n/a
7	chr7:6248449-6248499	AG09319	gingival:	n/a
8	chr7:6238486-6238536	GM12878	blood:	n/a
9	chr7:6218888-6218938	CMK	blood:	n/a
10	chr7:6248449-6248499	ovcar-3	ovarian:	n/a
11	chr7:6218888-6218938	HIPEpiC	eye:	n/a
12	chr7:6238486-6238536	HRCEpiC	kidney:	n/a
13	chr7:6238486-6238536	NHDF-neo	bronchial:	n/a
14	chr7:6238486-6238536	AG04450	lung:	fetal
15	chr7:6248449-6248499	SKMC	muscle:	n/a
16	chr7:6238486-6238536	HEK293	kidney:	embryo
17	chr7:6248449-6248499	HCM	heart:	n/a
18	chr7:6218888-6218938	SKMC	muscle:	n/a
19	chr7:6248449-6248499	GM12892	blood:	n/a
20	chr7:6238486-6238536	HPAEpiC	pulmonary alveolar:	n/a
21	chr7:6218888-6218938	LNCaP	prostate:	n/a
22	chr7:6218888-6218938	NT2-D1	testis:	n/a
23	chr7:6248449-6248499	Hepatocyte	liver:	n/a
24	chr7:6248449-6248499	BJ	skin:	n/a
25	chr7:6218888-6218938	HepG2	liver:	n/a
26	chr7:6238486-6238536	GM19239	blood:	n/a
27	chr7:6248449-6248499	AoSMC	blood vessel:	n/a
28	chr7:6248449-6248499	GM19239	blood:	n/a
29	chr7:6218888-6218938	SAEC	small airway:	n/a
30	chr7:6218888-6218938	HRE	kidney:	n/a
31	chr7:6218888-6218938	H1-hESC	embryonic stem cell:	embryo
32	chr7:6248449-6248499	HMEC	breast:	n/a
33	chr7:6218888-6218938	GM06990	blood:	n/a
34	chr7:6248449-6248499	PFSK-1	brain:	n/a
35	chr7:6248449-6248499	HEEpiC	esophagus:	n/a
36	chr7:6238486-6238536	HRPEpiC	eye:	n/a
37	chr7:6238486-6238536	AG10803	skin:	n/a
38	chr7:6238486-6238536	GM06990	blood:	n/a
39	chr7:6238486-6238536	U87	brain:	n/a
40	chr7:6218888-6218938	Hela-S3	cervix:	n/a
41	chr7:6248449-6248499	ECC-1	luminal epithelium:	n/a
42	chr7:6218888-6218938	RPTEC	kidney:	n/a
43	chr7:6248449-6248499	SK-N-SH_RA	brain:	n/a
44	chr7:6248449-6248499	MCF-7	breast:	n/a
45	chr7:6218888-6218938	ECC-1	luminal epithelium:	n/a
46	chr7:6238486-6238536	HUVEC	blood vessel:	n/a
47	chr7:6248449-6248499	SAEC	small airway:	n/a
48	chr7:6218888-6218938	PANC-1	pancreas:	n/a
49	chr7:6218888-6218938	AG10803	skin:	n/a
50	chr7:6238486-6238536	AoSMC	blood vessel:	n/a

(count:23 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:6218606..6220870-chr7:6221608..6224253,2	K562	blood:
2	chr7:6137902..6140709-chr7:6237423..6239773,2	K562	blood:
3	chr7:6218147..6221120-chr7:6228782..6230937,2	K562	blood:
4	chr7:6218147..6221120-chr7:6228782..6230937,2	K562	blood:
5	chr7:6236702..6238483-chr7:6243119..6244691,2	K562	blood:
6	chr7:6237378..6239314-chr7:6387267..6389950,2	MCF-7	breast:
7	chr7:6238671..6240280-chr7:6246179..6247952,2	K562	blood:
8	chr7:6238671..6240280-chr7:6246179..6247952,2	K562	blood:
9	chr7:6216897..6219662-chr7:6222027..6224471,2	MCF-7	breast:
10	chr7:6253410..6256369-chr7:6257945..6259887,2	K562	blood:
11	chr7:6231008..6235144-chr7:6239773..6243041,3	K562	blood:
12	chr7:6097168..6098982-chr7:6228350..6229954,2	MCF-7	breast:
13	chr7:6214344..6218044-chr7:6310010..6312416,3	MCF-7	breast:
14	chr7:6236702..6238483-chr7:6243119..6244691,2	K562	blood:
15	chr7:6231008..6235144-chr7:6239773..6243041,3	K562	blood:
16	chr7:6253410..6256369-chr7:6257945..6259887,2	K562	blood:
17	chr7:6217036..6219726-chr7:6310745..6313246,2	K562	blood:
18	chr7:6217505..6219217-chr7:6223350..6224980,2	MCF-7	breast:
19	chr7:6144209..6146088-chr7:6252754..6255605,2	K562	blood:
20	chr7:6218606..6220870-chr7:6221608..6224253,2	K562	blood:
21	chr7:6248788..6250767-chr7:6299120..6301643,2	MCF-7	breast:
22	chr7:6246409..6248092-chr7:6248165..6250514,2	K562	blood:
23	chr7:6246409..6248092-chr7:6248165..6250514,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000238534	TF binding region
CYTH3	TF binding region
ENSG00000202273	TF binding region
ENSG00000238534	CpG island
CYTH3	CpG island
ENSG00000202273	CpG island
ENSG00000008256	chromatin interactions
ENSG00000086232	chromatin interactions
ENSG00000106346	chromatin interactions
ENSG00000178397	chromatin interactions

Extended variants
information (count: 2225 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:2225 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs561545390	chr7:6217869-6217870	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs572791265	chr7:6217914-6217915	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs529553738	chr7:6217915-6217916	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs528939923	chr7:6217921-6217922	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs114471635	chr7:6217927-6217928	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs559518949	chr7:6217941-6217942	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs374776176	chr7:6217946-6217947	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs555517900	chr7:6217976-6217977	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs551692901	chr7:6217995-6217996	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs71531363	chr7:6218003-6218004	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs202043499	chr7:6218009-6218010	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs148385446	chr7:6218038-6218039	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs74602419	chr7:6218056-6218057	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs188210685	chr7:6218075-6218076	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs553542835	chr7:6218083-6218084	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs370438494	chr7:6218103-6218104	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs149442565	chr7:6218104-6218105	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs571775928	chr7:6218108-6218109	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs539570555	chr7:6218157-6218158	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs557686582	chr7:6218158-6218159	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs576251252	chr7:6218173-6218174	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs115034029	chr7:6218197-6218198	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs555319921	chr7:6218200-6218201	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs573350115	chr7:6218210-6218211	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs34054251	chr7:6218230-6218231	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs540719675	chr7:6218269-6218270	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs543264577	chr7:6218284-6218285	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs551455593	chr7:6218299-6218300	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs36096817	chr7:6218309-6218310	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs561128303	chr7:6218311-6218312	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs180777209	chr7:6218324-6218325	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs187325123	chr7:6218331-6218332	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs368769224	chr7:6218374-6218375	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs558983907	chr7:6218395-6218396	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs141402973	chr7:6218423-6218424	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs75480745	chr7:6218427-6218428	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs563749223	chr7:6218430-6218431	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs531223107	chr7:6218445-6218446	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs368278178	chr7:6218530-6218531	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs549441066	chr7:6218555-6218556	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs567653957	chr7:6218574-6218575	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs528452556	chr7:6218595-6218596	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs116360828	chr7:6218615-6218616	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs571738994	chr7:6218675-6218676	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs570045264	chr7:6218679-6218680	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs77734905	chr7:6218692-6218693	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs192226376	chr7:6218699-6218700	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs569777459	chr7:6218700-6218701	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs537347207	chr7:6218726-6218727	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs181880536	chr7:6218731-6218732	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:78)

Disease	PMID	Source
Lynch syndrome	22585707	CNVD
Follicular lymphoma	20505157	CNVD
Breast cancer	16397240	CNVD
Raine Syndrome	17924334	CNVD
Diffuse large b-cell lymphoma	21266526	CNVD
Melanoma	18172304	CNVD
Sudden cardiac death	19188705	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Glioma	18556773	CNVD
Ovarian cancer	21720365	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
Developmental delay	21147756	CNVD
Prostate cancer	18632612	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
Bladder cancer	21909424	CNVD
Myelofibrosis	22110671	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	21045282	CNVD
Disorders of sex development	21048976	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Acute myeloid leukemia	21251322	CNVD
small cell lung cancer	17426248	CNVD
Breast cancer	22522925	CNVD
Glioblastoma multiforme	21525872	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:982 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:6146800-6218200	Weak transcription	Stomach Mucosa	stomach
2	chr7:6184000-6218600	Strong transcription	Fetal Intestine Small	intestine
3	chr7:6198800-6220000	Weak transcription	Primary hematopoietic stem cells	blood
4	chr7:6199200-6219200	Weak transcription	H9 Cell Line	embryonic stem cell
5	chr7:6201400-6219200	Weak transcription	K562	blood
6	chr7:6201800-6226400	Weak transcription	Liver	Liver
7	chr7:6202000-6230600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
8	chr7:6202400-6218000	Weak transcription	Small Intestine	intestine
9	chr7:6202400-6226600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
10	chr7:6202400-6238000	Weak transcription	Fetal Kidney	kidney
11	chr7:6202600-6218000	Weak transcription	Psoas Muscle	Psoas
12	chr7:6202600-6228200	Weak transcription	Dnd41	blood
13	chr7:6203800-6218000	Weak transcription	Rectal Smooth Muscle	rectum
14	chr7:6204600-6228000	Weak transcription	Brain Cingulate Gyrus	brain
15	chr7:6207800-6229800	Weak transcription	Placenta Amnion	Placenta Amnion
16	chr7:6208200-6219600	Weak transcription	Fetal Thymus	thymus
17	chr7:6209600-6230000	Weak transcription	Cortex derived primary cultured neurospheres	brain
18	chr7:6209800-6218000	Weak transcription	Brain Angular Gyrus	brain
19	chr7:6210000-6219400	Weak transcription	Primary T helper cells fromperipheralblood	blood
20	chr7:6210000-6230000	Weak transcription	Brain Substantia Nigra	brain
21	chr7:6210200-6219200	Weak transcription	Fetal Brain Male	brain
22	chr7:6210600-6228000	Weak transcription	Thymus	Thymus
23	chr7:6210800-6229600	Weak transcription	Colonic Mucosa	Colon
24	chr7:6210800-6230000	Strong transcription	Fetal Stomach	stomach
25	chr7:6211000-6226200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
26	chr7:6211800-6237800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
27	chr7:6212000-6220400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
28	chr7:6212200-6219400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
29	chr7:6212200-6237800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
30	chr7:6212400-6218000	Strong transcription	HSMMtube	muscle
31	chr7:6212600-6220800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr7:6212600-6231000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr7:6212800-6219000	Weak transcription	HUES6 Cell Line	embryonic stem cell
34	chr7:6212800-6238200	Weak transcription	Brain Inferior Temporal Lobe	brain
35	chr7:6213000-6231200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
36	chr7:6213200-6218000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
37	chr7:6213200-6218000	Weak transcription	Brain Anterior Caudate	brain
38	chr7:6213200-6218000	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
39	chr7:6213200-6218000	Weak transcription	Spleen	Spleen
40	chr7:6213200-6219800	Weak transcription	Esophagus	oesophagus
41	chr7:6213200-6240600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr7:6214000-6219200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
43	chr7:6215400-6218000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
44	chr7:6215800-6218000	Strong transcription	HSMM	muscle
45	chr7:6215800-6218200	Strong transcription	Duodenum Mucosa	Duodenum
46	chr7:6215800-6220600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
47	chr7:6215800-6220600	Weak transcription	HUVEC	blood vessel
48	chr7:6215800-6220800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
49	chr7:6215800-6231400	Weak transcription	Hela-S3	cervix
50	chr7:6216000-6218000	Strong transcription	Osteobl	bone

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