Variant report

Variant	nsv1032311
Chromosome Location	chr8:6978399-7226424
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1067)
CpG islands
(count:2808)
Chromatin interactive
region (count:2)
LncRNA
region (count:13)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1067 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

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	chr8:7215685-7216141	GM12878	blood:	n/a	n/a
3	BATF	chr8:7016048-7016290	GM12878	blood:	n/a	n/a
4	BATF	chr8:7065286-7065896	GM12878	blood:	n/a	chr8:7065585-7065596
5	BATF	chr8:7212714-7213011	GM12878	blood:	n/a	n/a
6	BATF	chr8:7105978-7106319	GM12878	blood:	n/a	n/a
7	BATF	chr8:7106013-7106321	GM12878	blood:	n/a	n/a
8	BATF	chr8:7065329-7065744	GM12878	blood:	n/a	chr8:7065585-7065596
9	BATF	chr8:6998432-6998646	GM12878	blood:	n/a	n/a
10	BATF	chr8:7220356-7220781	GM12878	blood:	n/a	n/a
11	BATF	chr8:7215669-7216199	GM12878	blood:	n/a	n/a
12	BCL11A	chr8:7059717-7059897	GM12878	blood:	n/a	n/a
13	BCL11A	chr8:7220370-7220830	GM12878	blood:	n/a	n/a
14	BCL11A	chr8:7065285-7065931	GM12878	blood:	n/a	n/a
15	BCL11A	chr8:7078884-7079047	GM12878	blood:	n/a	n/a
16	BCL11A	chr8:7212700-7212924	GM12878	blood:	n/a	n/a
17	BCL11A	chr8:7065268-7065674	GM12878	blood:	n/a	n/a
18	BCL11A	chr8:7096016-7096195	GM12878	blood:	n/a	chr8:7096138-7096151
19	BCL11A	chr8:7213997-7214166	GM12878	blood:	n/a	n/a
20	BCL11A	chr8:7215704-7215862	GM12878	blood:	n/a	n/a
21	BCL3	chr8:7199106-7199270	GM12878	blood:	n/a	chr8:7199138-7199147
22	BHLHE40	chr8:7212714-7213011	GM12878	blood:	n/a	n/a
23	BHLHE40	chr8:7079428-7079694	HepG2	liver:	n/a	chr8:7079551-7079567
24	BHLHE40	chr8:7212724-7213120	K562	blood:	n/a	n/a
25	BRCA1	chr8:7212733-7213463	GM12878	blood:	n/a	n/a
26	CBX3	chr8:7009532-7009840	K562	blood:	n/a	n/a
27	CEBPB	chr8:7216733-7216933	HepG2	liver:	n/a	chr8:7216873-7216886 chr8:7216873-7216886 chr8:7216873-7216884
28	CEBPB	chr8:6990754-6990963	K562	blood:	n/a	n/a
29	CEBPB	chr8:6990758-6990880	H1-hESC	embryonic stem cell:	n/a	n/a
30	CEBPB	chr8:7005819-7006426	K562	blood:	n/a	n/a
31	CEBPB	chr8:6990652-6990853	K562	blood:	n/a	n/a
32	CEBPB	chr8:7178817-7179042	K562	blood:	n/a	n/a
33	CEBPB	chr8:7003781-7004139	K562	blood:	n/a	n/a
34	CEBPB	chr8:7005971-7006346	K562	blood:	n/a	n/a
35	CEBPB	chr8:7003837-7004114	K562	blood:	n/a	n/a
36	CEBPD	chr8:7005807-7006267	K562	blood:	n/a	n/a
37	CHD1	chr8:7212595-7213212	GM12878	blood:	n/a	n/a
38	CHD2	chr8:7154376-7154713	HepG2	liver:	n/a	n/a
39	CTCF	chr8:7161730-7161736	K562	blood:	n/a	n/a
40	CTCF	chr8:7161760-7161781	HUVEC	blood vessel:	n/a	n/a
41	CTCF	chr8:6983567-6983884	H1-hESC	embryonic stem cell:	n/a	chr8:6983718-6983731
42	CTCF	chr8:7212821-7213027	MCF-7	breast:	n/a	chr8:7212917-7212935 chr8:7212904-7212922 chr8:7212919-7212940
43	CTCF	chr8:7085540-7085690	HMEC	breast:	n/a	n/a
44	CTCF	chr8:7079556-7079706	HepG2	liver:	n/a	chr8:7079617-7079630 chr8:7079616-7079632 chr8:7079615-7079633 chr8:7079610-7079631 chr8:7079617-7079630
45	CTCF	chr8:7079488-7079759	Medullo	brain:	n/a	chr8:7079617-7079630 chr8:7079616-7079632 chr8:7079615-7079633 chr8:7079610-7079631 chr8:7079617-7079630
46	CTCF	chr8:7085572-7085947	K562	blood:	n/a	chr8:7085759-7085777 chr8:7085754-7085775 chr8:7085761-7085774 chr8:7085761-7085774 chr8:7085760-7085776
47	CTCF	chr8:7212880-7213030	BE2_C	brain:	n/a	chr8:7212917-7212935 chr8:7212904-7212922 chr8:7212919-7212940
48	CTCF	chr8:7212732-7213107	A549	lung:	n/a	chr8:7212917-7212935 chr8:7212904-7212922 chr8:7212919-7212940
49	CTCF	chr8:7212880-7213030	HFF	foreskin:	n/a	chr8:7212917-7212935 chr8:7212904-7212922 chr8:7212919-7212940
50	CTCF	chr8:7150139-7150440	K562	blood:	n/a	chr8:7150277-7150295

(count:2808 , 50 per page) page: 1 2 3 4 5 6 7 ... 57

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:7213526-7213576	HCPEpiC	choroid plexus:	n/a
2	chr8:7113417-7113467	NT2-D1	testis:	n/a
3	chr8:7213526-7213576	HCPEpiC	choroid plexus:	n/a
4	chr8:7113417-7113467	NT2-D1	testis:	n/a
5	chr8:7154895-7154945	GM19239	blood:	n/a
6	chr8:7155667-7155717	H1-hESC	embryonic stem cell:	embryo
7	chr8:7120562-7120612	PrEC	prostate:	n/a
8	chr8:7083881-7083931	SAEC	small airway:	n/a
9	chr8:7015931-7015981	HRE	kidney:	n/a
10	chr8:7005678-7005728	CMK	blood:	n/a
11	chr8:7144084-7144134	AG09319	gingival:	n/a
12	chr8:7212700-7212750	AG09319	gingival:	n/a
13	chr8:7079761-7079811	NT2-D1	testis:	n/a
14	chr8:7005011-7005061	AG09309	skin:	n/a
15	chr8:7212488-7212538	HL-60	blood:	n/a
16	chr8:7212954-7213004	GM06990	blood:	n/a
17	chr8:7191273-7191323	SK-N-MC	brain:	n/a
18	chr8:7005011-7005061	HCF	heart:	n/a
19	chr8:7085814-7085864	MCF-7	breast:	n/a
20	chr8:7083881-7083931	HRE	kidney:	n/a
21	chr8:7085602-7085652	NB4	blood:	n/a
22	chr8:7110581-7110631	NHDF-neo	bronchial:	n/a
23	chr8:7128706-7128756	MCF-7	breast:	n/a
24	chr8:7216871-7216921	Jurkat	blood:	n/a
25	chr8:7212954-7213004	SKMC	muscle:	n/a
26	chr8:7151550-7151600	HepG2	liver:	n/a
27	chr8:7154895-7154945	MCF-7	breast:	n/a
28	chr8:7155225-7155275	AG04449	skin:	fetal
29	chr8:7192145-7192195	SAEC	small airway:	n/a
30	chr8:7009699-7009749	HPAEpiC	pulmonary alveolar:	n/a
31	chr8:7005011-7005061	BE2_C	brain:	n/a
32	chr8:7155225-7155275	HepG2	liver:	n/a
33	chr8:7079761-7079811	HNPCEpiC	eye:	n/a
34	chr8:7156743-7156793	HIPEpiC	eye:	n/a
35	chr8:7005011-7005061	HMEC	breast:	n/a
36	chr8:7004944-7004994	AG10803	skin:	n/a
37	chr8:7004738-7004788	MCF10A-Er-Src	breast:	n/a
38	chr8:7153933-7153983	HAEpiC	amniotic membrane:	n/a
39	chr8:7079037-7079087	SK-N-MC	brain:	n/a
40	chr8:7005011-7005061	ovcar-3	ovarian:	n/a
41	chr8:7157397-7157447	HCF	heart:	n/a
42	chr8:7189580-7189630	HEK293	kidney:	embryo
43	chr8:7153685-7153735	T-47D	breast:	n/a
44	chr8:7079106-7079156	AG09319	gingival:	n/a
45	chr8:7191920-7191970	ProgFib	skin:	n/a
46	chr8:7144084-7144134	Hepatocyte	liver:	n/a
47	chr8:7005562-7005612	H1-hESC	embryonic stem cell:	embryo
48	chr8:7005011-7005061	HPAEpiC	pulmonary alveolar:	n/a
49	chr8:7155225-7155275	Hela-S3	cervix:	n/a
50	chr8:7213526-7213576	LNCaP	prostate:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:7079344..7079857-chr8:7537961..7538472,3	MCF-7	breast:
2	chr12:8332362..8333276-chr8:7212481..7212992,2	MCF-7	breast:

(count:13 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF705G-1	chr8:7212333-7212574	NONHSAT124826
2	lnc-ZNF705G-1	chr8:7206605-7206668	NONHSAT124824
3	lnc-DEFB105B-4	chr8:7010239-7010328	NONHSAT124814
4	lnc-ZNF705G-1	chr8:7181819-7181886	NONHSAT124824
5	lnc-ZNF705G-1	chr8:7182659-7182720	NONHSAT124824
6	lnc-DEFA5-2	chr8:7001154-7001363	NONHSAT124813
7	lnc-ZNF705G-1	chr8:7212333-7212511	NONHSAT124824
8	lnc-DEFB105B-4	chr8:7043806-7044422	NONHSAT124814
9	lnc-ZNF705G-1	chr8:7180835-7180882	NONHSAT124824
10	lnc-ZNF705G-1	chr8:7206593-7206668	NONHSAT124826
11	lnc-ZNF705G-1	chr8:7182344-7182411	NONHSAT124824
12	lnc-DEFB105B-3	chr8:7170368-7170425	NONHSAT124823
13	lnc-DEFB105B-3	chr8:7177268-7177473	NONHSAT124823

No data

Variant related genes	Relation type
FAM90A13P	TF binding region
FAM90A20P	TF binding region
DEFB109P1B	TF binding region
ENSG00000235778	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
DEFB108P2	TF binding region
ENSG00000254683	TF binding region
FAM90A5P	TF binding region
ENSG00000216206	TF binding region
ZNF705G	TF binding region
ENSG00000231930	TF binding region
OR7E125P	TF binding region
FAM66B	TF binding region
RPS3AP30	TF binding region
USP17L1P	TF binding region
USP17L4	TF binding region
FAM90A13P	CpG island
FAM90A20P	CpG island
DEFB109P1B	CpG island
ENSG00000235778	CpG island
ENSG00000221567	CpG island
ENSG00000230106	CpG island
ENSG00000255025	CpG island
FAM90A3P	CpG island
RPS3AP33	CpG island
FAM90A4P	CpG island
FAM90A15P	CpG island
DEFB108P2	CpG island
ENSG00000254683	CpG island
FAM90A5P	CpG island
ENSG00000216206	CpG island
ZNF705G	CpG island
ENSG00000231930	CpG island
OR7E125P	CpG island
FAM66B	CpG island
RPS3AP30	CpG island
USP17L1P	CpG island
USP17L4	CpG island
ENSG00000226711	chromatin interactions

Extended variants
information (count: 3454 )
Associated
traits (count: 153 )

Variant overlapped rSNPs/rCNVs (count:3454 , 50 per page) page: 1 2 3 4 5 6 7 ... 70

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs200415169	chr8:6979720-6979721	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs201453361	chr8:6979722-6979723	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs564514937	chr8:6979763-6979764	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs532961904	chr8:6979764-6979765	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs185077659	chr8:6979768-6979769	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs201178876	chr8:6979777-6979778	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs541325589	chr8:6979780-6979781	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs561537316	chr8:6979786-6979787	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs530206631	chr8:6979793-6979794	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs180858204	chr8:6985002-6985003	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs542891834	chr8:6985013-6985014	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs371726274	chr8:6985024-6985025	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs577710665	chr8:6985025-6985026	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs545521501	chr8:6985037-6985038	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs552059183	chr8:6985048-6985049	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs13257767	chr8:6985058-6985059	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs530948177	chr8:6985075-6985076	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs369652715	chr8:6985076-6985077	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs567804549	chr8:6985077-6985078	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs528855619	chr8:6985081-6985082	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs535637345	chr8:6985083-6985084	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs186498577	chr8:6985089-6985090	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs565877763	chr8:6985091-6985092	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs71509248	chr8:6985095-6985096	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs377215076	chr8:6985098-6985099	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs557653089	chr8:6985099-6985100	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs577196146	chr8:6985101-6985102	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs536681901	chr8:6985103-6985104	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs556629025	chr8:6985105-6985106	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs369983286	chr8:6985119-6985120	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs562877439	chr8:6985120-6985121	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs573447731	chr8:6985121-6985122	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs191340626	chr8:6985124-6985125	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs573399491	chr8:6985147-6985148	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs545346317	chr8:6985158-6985159	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs149688607	chr8:6985172-6985173	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs182578688	chr8:6985173-6985174	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs551044137	chr8:6985175-6985176	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs551604869	chr8:6985176-6985177	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs187578271	chr8:6985184-6985185	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs530099884	chr8:6985188-6985189	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs547088616	chr8:6985190-6985191	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs565708834	chr8:6985197-6985198	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs534846797	chr8:6985198-6985199	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs551246156	chr8:6985205-6985206	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs147806030	chr8:6985217-6985218	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs190487950	chr8:6985221-6985222	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs556491397	chr8:6985230-6985231	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs527794445	chr8:6985232-6985233	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs535930113	chr8:6985236-6985237	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:153)

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
Myxofibrosarcoma	16751306	CNVD
Immune disease	21572526	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Kallmann Syndrome 2	22470819	CNVD

Chromatin state (count:284 , 50 per page) page: 1 2 3 4 5 6

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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