Variant report

Variant	nsv1026699
Chromosome Location	chr8:6969814-7186634
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	BACH1	chr8:7085606-7085806	H1-hESC	embryonic stem cell:	n/a	n/a
2	BATF	chr8:6976169-6976555	GM12878	blood:	n/a	n/a
3	BATF	chr8:7016048-7016290	GM12878	blood:	n/a	n/a
4	BATF	chr8:7105978-7106319	GM12878	blood:	n/a	n/a
5	BATF	chr8:7106013-7106321	GM12878	blood:	n/a	n/a
6	BATF	chr8:7065286-7065896	GM12878	blood:	n/a	chr8:7065585-7065596
7	BATF	chr8:6976187-6976452	GM12878	blood:	n/a	n/a
8	BATF	chr8:6998432-6998646	GM12878	blood:	n/a	n/a
9	BATF	chr8:7065329-7065744	GM12878	blood:	n/a	chr8:7065585-7065596
10	BCL11A	chr8:7078884-7079047	GM12878	blood:	n/a	n/a
11	BCL11A	chr8:6975956-6976114	GM12878	blood:	n/a	n/a
12	BCL11A	chr8:7096016-7096195	GM12878	blood:	n/a	chr8:7096138-7096151
13	BCL11A	chr8:7065268-7065674	GM12878	blood:	n/a	n/a
14	BCL11A	chr8:7065285-7065931	GM12878	blood:	n/a	n/a
15	BCL11A	chr8:7059717-7059897	GM12878	blood:	n/a	n/a
16	BHLHE40	chr8:7079428-7079694	HepG2	liver:	n/a	chr8:7079551-7079567
17	CBX3	chr8:7009532-7009840	K562	blood:	n/a	n/a
18	CEBPB	chr8:7003781-7004139	K562	blood:	n/a	n/a
19	CEBPB	chr8:7178817-7179042	K562	blood:	n/a	n/a
20	CEBPB	chr8:7005971-7006346	K562	blood:	n/a	n/a
21	CEBPB	chr8:7005819-7006426	K562	blood:	n/a	n/a
22	CEBPB	chr8:6990754-6990963	K562	blood:	n/a	n/a
23	CEBPB	chr8:7003837-7004114	K562	blood:	n/a	n/a
24	CEBPB	chr8:6990758-6990880	H1-hESC	embryonic stem cell:	n/a	n/a
25	CEBPB	chr8:6990652-6990853	K562	blood:	n/a	n/a
26	CEBPD	chr8:7005807-7006267	K562	blood:	n/a	n/a
27	CHD2	chr8:7154376-7154713	HepG2	liver:	n/a	n/a
28	CTCF	chr8:7085560-7085710	GM12878	blood:	n/a	n/a
29	CTCF	chr8:7085670-7085897	GM19238	blood:	n/a	chr8:7085759-7085777 chr8:7085754-7085775 chr8:7085761-7085774 chr8:7085761-7085774 chr8:7085760-7085776
30	CTCF	chr8:7085560-7085710	HCM	heart:	n/a	n/a
31	CTCF	chr8:7112026-7112326	K562	blood:	n/a	chr8:7112166-7112184
32	CTCF	chr8:7085697-7085867	HUVEC	blood vessel:	n/a	chr8:7085759-7085777 chr8:7085754-7085775 chr8:7085761-7085774 chr8:7085761-7085774 chr8:7085760-7085776
33	CTCF	chr8:7161721-7161824	Gliobla	brain:	n/a	chr8:7161752-7161773 chr8:7161757-7161775
34	CTCF	chr8:7176851-7176999	GM10248	blood:	n/a	chr8:7176908-7176929 chr8:7176906-7176924
35	CTCF	chr8:7079640-7079790	GM12874	blood:	n/a	n/a
36	CTCF	chr8:7079574-7079697	HUVEC	blood vessel:	n/a	chr8:7079617-7079630 chr8:7079616-7079632 chr8:7079615-7079633 chr8:7079610-7079631 chr8:7079617-7079630
37	CTCF	chr8:7176876-7176908	GM19239	blood:	n/a	n/a
38	CTCF	chr8:7085639-7085951	Spleen_OC	spleen:	n/a	chr8:7085759-7085777 chr8:7085754-7085775 chr8:7085761-7085774 chr8:7085761-7085774 chr8:7085760-7085776
39	CTCF	chr8:7079640-7079790	HAc	cerebellar:	n/a	n/a
40	CTCF	chr8:7150113-7150460	K562	blood:	n/a	chr8:7150277-7150295
41	CTCF	chr8:7079464-7079794	K562	blood:	n/a	chr8:7079617-7079630 chr8:7079616-7079632 chr8:7079615-7079633 chr8:7079610-7079631 chr8:7079617-7079630
42	CTCF	chr8:7181774-7181865	GM10248	blood:	n/a	n/a
43	CTCF	chr8:7079394-7079782	K562	blood:	n/a	chr8:7079617-7079630 chr8:7079616-7079632 chr8:7079615-7079633 chr8:7079610-7079631 chr8:7079617-7079630
44	CTCF	chr8:7079529-7079693	Spleen_OC	spleen:	n/a	chr8:7079617-7079630 chr8:7079616-7079632 chr8:7079615-7079633 chr8:7079610-7079631 chr8:7079617-7079630
45	CTCF	chr8:7161692-7161833	MCF-7	breast:	n/a	chr8:7161752-7161773 chr8:7161757-7161775
46	CTCF	chr8:7079480-7079728	Lung_OC	lung:	n/a	chr8:7079617-7079630 chr8:7079616-7079632 chr8:7079615-7079633 chr8:7079610-7079631 chr8:7079617-7079630
47	CTCF	chr8:7079640-7079790	HUVEC	blood vessel:	n/a	n/a
48	CTCF	chr8:6983680-6983830	Caco-2	colon:	n/a	chr8:6983718-6983731
49	CTCF	chr8:7085615-7085894	IMR90	lung:	n/a	chr8:7085759-7085777 chr8:7085754-7085775 chr8:7085761-7085774 chr8:7085761-7085774 chr8:7085760-7085776
50	CTCF	chr8:7176820-7176927	HUVEC	blood vessel:	n/a	chr8:7176906-7176924

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:7113417-7113467	U87	brain:	n/a
2	chr8:7078402-7078452	Hepatocyte	liver:	n/a
3	chr8:7153933-7153983	HCM	heart:	n/a
4	chr8:7155667-7155717	Jurkat	blood:	n/a
5	chr8:7015931-7015981	ProgFib	skin:	n/a
6	chr8:7085814-7085864	HMEC	breast:	n/a
7	chr8:7085602-7085652	GM06990	blood:	n/a
8	chr8:7155667-7155717	SK-N-MC	brain:	n/a
9	chr8:7151550-7151600	T-47D	breast:	n/a
10	chr8:7079106-7079156	NHDF-neo	bronchial:	n/a
11	chr8:7079761-7079811	H1-hESC	embryonic stem cell:	embryo
12	chr8:7128706-7128756	NH-A	brain:	n/a
13	chr8:7110581-7110631	MCF-7	breast:	n/a
14	chr8:7085602-7085652	AG10803	skin:	n/a
15	chr8:7079106-7079156	K562	blood:	n/a
16	chr8:7079106-7079156	Jurkat	blood:	n/a
17	chr8:7151550-7151600	U87	brain:	n/a
18	chr8:7120562-7120612	HEK293	kidney:	embryo
19	chr8:7155225-7155275	SAEC	small airway:	n/a
20	chr8:7151550-7151600	HRE	kidney:	n/a
21	chr8:7153933-7153983	NT2-D1	testis:	n/a
22	chr8:7120562-7120612	NHBE	bronchial:	n/a
23	chr8:7154895-7154945	PANC-1	pancreas:	n/a
24	chr8:7156743-7156793	SK-N-SH	brain:	n/a
25	chr8:7155667-7155717	HIPEpiC	eye:	n/a
26	chr8:7155667-7155717	HPAEpiC	pulmonary alveolar:	n/a
27	chr8:7144084-7144134	SK-N-SH_RA	brain:	n/a
28	chr8:7157397-7157447	BE2_C	brain:	n/a
29	chr8:7155225-7155275	Hela-S3	cervix:	n/a
30	chr8:7076476-7076526	HCM	heart:	n/a
31	chr8:7151550-7151600	RPTEC	kidney:	n/a
32	chr8:7110581-7110631	LNCaP	prostate:	n/a
33	chr8:7120562-7120612	IMR90	lung:	fetal
34	chr8:7004738-7004788	AG04450	lung:	fetal
35	chr8:7079037-7079087	SK-N-MC	brain:	n/a
36	chr8:7120562-7120612	HRCEpiC	kidney:	n/a
37	chr8:7004738-7004788	ovcar-3	ovarian:	n/a
38	chr8:7085602-7085652	HRPEpiC	eye:	n/a
39	chr8:7155667-7155717	BJ	skin:	n/a
40	chr8:7085814-7085864	HEK293	kidney:	embryo
41	chr8:7076476-7076526	Hela-S3	cervix:	n/a
42	chr8:7085602-7085652	NB4	blood:	n/a
43	chr8:7153933-7153983	HRE	kidney:	n/a
44	chr8:7120562-7120612	SAEC	small airway:	n/a
45	chr8:7083881-7083931	RPTEC	kidney:	n/a
46	chr8:7009699-7009749	GM12878	blood:	n/a
47	chr8:7110581-7110631	T-47D	breast:	n/a
48	chr8:7005678-7005728	AoSMC	blood vessel:	n/a
49	chr8:7005562-7005612	AoSMC	blood vessel:	n/a
50	chr8:7004944-7004994	ProgFib	skin:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:7079344..7079857-chr8:7537961..7538472,3	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF705G-1	chr8:7182344-7182411	NONHSAT124824
2	lnc-DEFB105B-4	chr8:7043806-7044422	NONHSAT124814
3	lnc-ZNF705G-1	chr8:7182659-7182720	NONHSAT124824
4	lnc-DEFB105B-4	chr8:7010239-7010328	NONHSAT124814
5	lnc-ZNF705G-1	chr8:7180835-7180882	NONHSAT124824
6	lnc-DEFB105B-3	chr8:7177268-7177473	NONHSAT124823
7	lnc-DEFB105B-3	chr8:7170368-7170425	NONHSAT124823
8	lnc-ZNF705G-1	chr8:7181819-7181886	NONHSAT124824
9	lnc-DEFA5-2	chr8:7001154-7001363	NONHSAT124813

Variant related genes	Relation type
FAM90A13P	TF binding region
ENSG00000234120	TF binding region
FAM90A20P	TF binding region
DEFB109P1B	TF binding region
ENSG00000221567	TF binding region
ENSG00000230106	TF binding region
ENSG00000255025	TF binding region
FAM90A3P	TF binding region
RPS3AP33	TF binding region
FAM90A4P	TF binding region
FAM90A15P	TF binding region
ENSG00000254683	TF binding region
FAM90A5P	TF binding region
ENSG00000216206	TF binding region
ENSG00000231930	TF binding region
OR7E125P	TF binding region
RPS3AP30	TF binding region
USP17L1P	TF binding region
FAM90A13P	CpG island
ENSG00000234120	CpG island
FAM90A20P	CpG island
DEFB109P1B	CpG island
ENSG00000221567	CpG island
ENSG00000230106	CpG island
ENSG00000255025	CpG island
FAM90A3P	CpG island
RPS3AP33	CpG island
FAM90A4P	CpG island
FAM90A15P	CpG island
ENSG00000254683	CpG island
FAM90A5P	CpG island
ENSG00000216206	CpG island
ENSG00000231930	CpG island
OR7E125P	CpG island
RPS3AP30	CpG island
USP17L1P	CpG island

Extended variants
information (count: 2433 )
Associated
traits (count: 148 )

Variant overlapped rSNPs/rCNVs (count:2433 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs200510751	chr8:6971251-6971252	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs529050150	chr8:6971252-6971253	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs193030055	chr8:6971262-6971263	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs201711432	chr8:6971265-6971266	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs538541102	chr8:6971270-6971271	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs559650443	chr8:6971271-6971272	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs184937882	chr8:6971273-6971274	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs551335535	chr8:6971289-6971290	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs189464811	chr8:6971304-6971305	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs537060035	chr8:6971309-6971310	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs141037407	chr8:6971313-6971314	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs191593767	chr8:6971316-6971317	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs183719395	chr8:6971328-6971329	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs189947742	chr8:6971329-6971330	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs372340888	chr8:6971330-6971331	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs553186804	chr8:6971335-6971336	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs573463257	chr8:6971350-6971351	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs539008184	chr8:6971363-6971364	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs201174273	chr8:6971393-6971394	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs181343528	chr8:6971403-6971404	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs186353321	chr8:6971410-6971411	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs575506629	chr8:6971414-6971415	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs190023629	chr8:6971423-6971424	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs536603099	chr8:6971462-6971463	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs80249871	chr8:6971473-6971474	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs367710107	chr8:6971477-6971478	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs35965487	chr8:6971478-6971479	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs200550862	chr8:6971498-6971499	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs556907793	chr8:6971504-6971505	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs537521271	chr8:6971517-6971518	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs569593701	chr8:6974938-6974939	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
32	rs538209696	chr8:6974959-6974960	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
33	rs115156553	chr8:6974960-6974961	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
34	rs144446568	chr8:6974975-6974976	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
35	rs146609740	chr8:6974976-6974977	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
36	rs141272256	chr8:6974983-6974984	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
37	rs572945580	chr8:6974988-6974989	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
38	rs574217446	chr8:6974991-6974992	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
39	rs530629620	chr8:6974995-6974996	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
40	rs181022132	chr8:6975033-6975034	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
41	rs558394069	chr8:6975034-6975035	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
42	rs544462678	chr8:6975046-6975047	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
43	rs143301913	chr8:6975058-6975059	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
44	rs186006187	chr8:6975061-6975062	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
45	rs372318964	chr8:6975091-6975092	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
46	rs560988015	chr8:6975134-6975135	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
47	rs574441123	chr8:6975146-6975147	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
48	rs375702707	chr8:6975172-6975173	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
49	rs369006552	chr8:6975382-6975383	Inactive region	TF binding region	3 gene(s)	Overlapped CNVs	n/a
50	rs532072274	chr8:6975415-6975416	Inactive region	TF binding region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:148)

Disease	PMID	Source
Ovarian clear cell carcinoma	21343371	CNVD
abnormal development	18461090	CNVD
Crohn''s disease	19220326	CNVD
Psoriasis	19220326	CNVD
Prostate cancer	21965145	CNVD
Prostate cancer	18515986	CNVD
Chronic obstructive pulmonary disease	20378733	CNVD
Autism	18414403	CNVD
Cancer	21183584	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Breast cancer	17603634	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Ovarian cancer	20844748	CNVD
Cervical cancer	17311676	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Schizophrenia	20877625	CNVD
Disorders of sex development	21048976	CNVD
Colorectal cancer	16272173	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Breast cancer	17001317	CNVD
Thyroid cancer	19087340	CNVD
Multiple myeloma	16616336	CNVD
Hepatocellular carcinoma	22174799	CNVD
Heart disease	21282601	CNVD
Prostate cancer	16573809	CNVD
T-cell lymphomas	19863542	CNVD
Ovarian cancer	22174824	CNVD
Colorectal cancer	21297112	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	17133270	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Breast cancer	17393978	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Breast cancer	20837533	CNVD
Squamous cell cancer	21044232	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	22429812	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Basal cell lymphoma	21115979	CNVD
Breast cancer	21264507	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Oral cancer	21386901	CNVD
Prostate cancer	21088497	CNVD
Breast cancer	20940404	CNVD
Colorectal cancer	19359472	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Gastric cancer	17167181	CNVD
Prostate cancer	16705090	CNVD
8p-syndrome	17576883	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Prostate cancer	17245344	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Cancer	16751803	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Breast cancer	21785460	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21509527	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Epilepsy	22083797	CNVD
Acute myeloid leukemia	21251322	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Congenital diaphragmatic hernia	21064195	CNVD
Autism	22495311	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16608533	CNVD
Seminomas	18059402	CNVD
Lung cancer	18438408	CNVD
Colorectal cancer	16774939	CNVD
Lung squamous cell carcinoma	22363434	CNVD
Cancer	20164919	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21364760	CNVD
Gastric cancer	18160780	CNVD
Breast cancer	21990379	CNVD
Psoriasis	20403174	CNVD
Psoriasis	20663923	CNVD
Crohn''s disease	16909382	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Crohn''s disease	20877625	CNVD
Inflammatory disorder	20877625	CNVD
Cardiac defect	21933911	CNVD
Psoriasis	18059266	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Psoriasis	20877625	CNVD
Mental retardation	17847001	CNVD
Prostate cancer	17217626	CNVD
Schizophrenia	21399695	CNVD
Colorectal cancer	21128281	CNVD
Colorectal cancer	19455253	CNVD
Psoriasis	18848619	CNVD
Squamous cell cancer	19047905	CNVD
Colorectal cancer	17229543	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Bladder cancer	21909424	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Cognitive impairment	21505072	CNVD
Breast cancer	17142309	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Schizophrenia	20967226	CNVD
small cell lung cancer	20016488	CNVD
Incontinentia Pigmenti	22033527	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Williams Syndrome	20824207	CNVD
Breast cancer	22522925	CNVD
Breast cancer	20369283	CNVD
Urothelial carcinoma	21177765	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Barrett''s syndrome	19417022	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:133 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:6985000-6985400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr8:6995000-6995600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
3	chr8:6995600-6996400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr8:6997000-7002200	Weak transcription	Dnd41	blood
5	chr8:6998600-6998800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
6	chr8:7001600-7004800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
7	chr8:7002200-7005000	Strong transcription	Dnd41	blood
8	chr8:7004800-7005000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
9	chr8:7005000-7011600	Weak transcription	Dnd41	blood
10	chr8:7006000-7011400	Weak transcription	HUES6 Cell Line	embryonic stem cell
11	chr8:7008800-7009200	Enhancers	Fetal Heart	heart
12	chr8:7009200-7010200	Weak transcription	Fetal Heart	heart
13	chr8:7009200-7011600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
14	chr8:7009800-7010400	Enhancers	H9 Cell Line	embryonic stem cell
15	chr8:7010200-7010400	Weak transcription	HUES64 Cell Line	embryonic stem cell
16	chr8:7010200-7010400	Enhancers	iPS-18 Cell Line	embryonic stem cell
17	chr8:7010400-7010600	Enhancers	HUES48 Cell Line	embryonic stem cell
18	chr8:7010400-7010600	Enhancers	HUES64 Cell Line	embryonic stem cell
19	chr8:7010400-7010600	Enhancers	iPS-15b Cell Line	embryonic stem cell
20	chr8:7010400-7010600	Enhancers	Fetal Heart	heart
21	chr8:7010400-7014600	Weak transcription	H9 Cell Line	embryonic stem cell
22	chr8:7010400-7014600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
23	chr8:7010600-7011600	Weak transcription	HUES48 Cell Line	embryonic stem cell
24	chr8:7010600-7014600	Weak transcription	HUES64 Cell Line	embryonic stem cell
25	chr8:7010600-7014600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
26	chr8:7011200-7013400	Weak transcription	H1 Cell Line	embryonic stem cell
27	chr8:7011400-7012600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr8:7011400-7012600	Strong transcription	HUES6 Cell Line	embryonic stem cell
29	chr8:7011600-7012200	Strong transcription	iPS-20b Cell Line	embryonic stem cell
30	chr8:7011600-7012400	Strong transcription	HUES48 Cell Line	embryonic stem cell
31	chr8:7011600-7012400	Strong transcription	Dnd41	blood
32	chr8:7012200-7014600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
33	chr8:7012400-7012600	Enhancers	ES-I3 Cell Line	embryonic stem cell
34	chr8:7012400-7014200	Weak transcription	Dnd41	blood
35	chr8:7012400-7015000	Weak transcription	HUES48 Cell Line	embryonic stem cell
36	chr8:7012600-7014800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
37	chr8:7012600-7015000	Weak transcription	HUES6 Cell Line	embryonic stem cell
38	chr8:7014600-7014800	Enhancers	iPS-18 Cell Line	embryonic stem cell
39	chr8:7014600-7014800	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
40	chr8:7014600-7015800	Active TSS	HUES64 Cell Line	embryonic stem cell
41	chr8:7014600-7015800	Active TSS	iPS-15b Cell Line	embryonic stem cell
42	chr8:7014600-7016000	Active TSS	H9 Cell Line	embryonic stem cell
43	chr8:7014800-7015000	Enhancers	ES-I3 Cell Line	embryonic stem cell
44	chr8:7014800-7016000	Active TSS	iPS-18 Cell Line	embryonic stem cell
45	chr8:7014800-7016000	Active TSS	iPS-20b Cell Line	embryonic stem cell
46	chr8:7015000-7015800	Active TSS	ES-I3 Cell Line	embryonic stem cell
47	chr8:7015000-7015800	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
48	chr8:7015000-7015800	Active TSS	HUES48 Cell Line	embryonic stem cell
49	chr8:7015000-7016000	Active TSS	HUES6 Cell Line	embryonic stem cell
50	chr8:7015400-7016000	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell

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