Variant report

Variant	nsv1033014
Chromosome Location	chr8:6959821-7226424
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1172)
CpG islands
(count:2810)
Chromatin interactive
region (count:2)
LncRNA
region (count:13)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1172 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

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	chr8:7016048-7016290	GM12878	blood:	n/a	n/a
3	BATF	chr8:7106013-7106321	GM12878	blood:	n/a	n/a
4	BATF	chr8:6998432-6998646	GM12878	blood:	n/a	n/a
5	BATF	chr8:6976169-6976555	GM12878	blood:	n/a	n/a
6	BATF	chr8:7215685-7216141	GM12878	blood:	n/a	n/a
7	BATF	chr8:7105978-7106319	GM12878	blood:	n/a	n/a
8	BATF	chr8:7215669-7216199	GM12878	blood:	n/a	n/a
9	BATF	chr8:7065329-7065744	GM12878	blood:	n/a	chr8:7065585-7065596
10	BATF	chr8:7220356-7220781	GM12878	blood:	n/a	n/a
11	BATF	chr8:6976187-6976452	GM12878	blood:	n/a	n/a
12	BATF	chr8:7212714-7213011	GM12878	blood:	n/a	n/a
13	BATF	chr8:7065286-7065896	GM12878	blood:	n/a	chr8:7065585-7065596
14	BCL11A	chr8:7096016-7096195	GM12878	blood:	n/a	chr8:7096138-7096151
15	BCL11A	chr8:7065285-7065931	GM12878	blood:	n/a	n/a
16	BCL11A	chr8:7078884-7079047	GM12878	blood:	n/a	n/a
17	BCL11A	chr8:7059717-7059897	GM12878	blood:	n/a	n/a
18	BCL11A	chr8:7220370-7220830	GM12878	blood:	n/a	n/a
19	BCL11A	chr8:6963128-6963505	GM12878	blood:	n/a	n/a
20	BCL11A	chr8:7212700-7212924	GM12878	blood:	n/a	n/a
21	BCL11A	chr8:6963184-6963444	GM12878	blood:	n/a	n/a
22	BCL11A	chr8:7215704-7215862	GM12878	blood:	n/a	n/a
23	BCL11A	chr8:7213997-7214166	GM12878	blood:	n/a	n/a
24	BCL11A	chr8:6975956-6976114	GM12878	blood:	n/a	n/a
25	BCL11A	chr8:7065268-7065674	GM12878	blood:	n/a	n/a
26	BCL3	chr8:7199106-7199270	GM12878	blood:	n/a	chr8:7199138-7199147
27	BHLHE40	chr8:7212714-7213011	GM12878	blood:	n/a	n/a
28	BHLHE40	chr8:7079428-7079694	HepG2	liver:	n/a	chr8:7079551-7079567
29	BHLHE40	chr8:7212724-7213120	K562	blood:	n/a	n/a
30	BRCA1	chr8:7212733-7213463	GM12878	blood:	n/a	n/a
31	CBX3	chr8:7009532-7009840	K562	blood:	n/a	n/a
32	CEBPB	chr8:7005971-7006346	K562	blood:	n/a	n/a
33	CEBPB	chr8:7005819-7006426	K562	blood:	n/a	n/a
34	CEBPB	chr8:7003781-7004139	K562	blood:	n/a	n/a
35	CEBPB	chr8:7178817-7179042	K562	blood:	n/a	n/a
36	CEBPB	chr8:6990754-6990963	K562	blood:	n/a	n/a
37	CEBPB	chr8:7003837-7004114	K562	blood:	n/a	n/a
38	CEBPB	chr8:7216733-7216933	HepG2	liver:	n/a	chr8:7216873-7216886 chr8:7216873-7216886 chr8:7216873-7216884
39	CEBPB	chr8:6990758-6990880	H1-hESC	embryonic stem cell:	n/a	n/a
40	CEBPB	chr8:6990652-6990853	K562	blood:	n/a	n/a
41	CEBPD	chr8:7005807-7006267	K562	blood:	n/a	n/a
42	CHD1	chr8:7212595-7213212	GM12878	blood:	n/a	n/a
43	CHD2	chr8:7154376-7154713	HepG2	liver:	n/a	n/a
44	CTCF	chr8:6966259-6966381	HepG2	liver:	n/a	n/a
45	CTCF	chr8:7068586-7068659	Pancreas_OC	pancreas:	n/a	n/a
46	CTCF	chr8:7111056-7111164	K562	blood:	n/a	n/a
47	CTCF	chr8:7079505-7079735	GM20000	blood:	n/a	chr8:7079617-7079630 chr8:7079616-7079632 chr8:7079615-7079633 chr8:7079610-7079631 chr8:7079617-7079630
48	CTCF	chr8:7213160-7213310	WI-38	lung:	n/a	n/a
49	CTCF	chr8:7212805-7213034	K562	blood:	n/a	chr8:7212917-7212935 chr8:7212904-7212922 chr8:7212919-7212940
50	CTCF	chr8:7015452-7015527	GM13976	blood:	n/a	n/a

(count:2810 , 50 per page) page: 1 2 3 4 5 6 7 ... 57

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:7212954-7213004	HCPEpiC	choroid plexus:	n/a
2	chr8:7208812-7208862	NB4	blood:	n/a
3	chr8:7079106-7079156	H1-hESC	embryonic stem cell:	embryo
4	chr8:7213999-7214049	ovcar-3	ovarian:	n/a
5	chr8:7212954-7213004	HCPEpiC	choroid plexus:	n/a
6	chr8:7208812-7208862	NB4	blood:	n/a
7	chr8:7079106-7079156	H1-hESC	embryonic stem cell:	embryo
8	chr8:7213999-7214049	ovcar-3	ovarian:	n/a
9	chr8:7113462-7113512	Jurkat	blood:	n/a
10	chr8:7192145-7192195	AG09319	gingival:	n/a
11	chr8:7085814-7085864	LNCaP	prostate:	n/a
12	chr8:7157397-7157447	SAEC	small airway:	n/a
13	chr8:7221471-7221521	T-47D	breast:	n/a
14	chr8:7005678-7005728	NHBE	bronchial:	n/a
15	chr8:7212700-7212750	HRE	kidney:	n/a
16	chr8:7113417-7113467	HRPEpiC	eye:	n/a
17	chr8:7005562-7005612	HCT-116	colon:	n/a
18	chr8:7004819-7004869	AG09309	skin:	n/a
19	chr8:7192145-7192195	GM12878	blood:	n/a
20	chr8:7208812-7208862	HPAEpiC	pulmonary alveolar:	n/a
21	chr8:7212954-7213004	PANC-1	pancreas:	n/a
22	chr8:7005678-7005728	GM12891	blood:	n/a
23	chr8:7156743-7156793	HepG2	liver:	n/a
24	chr8:7156743-7156793	PANC-1	pancreas:	n/a
25	chr8:7212954-7213004	MCF10A-Er-Src	breast:	n/a
26	chr8:7208812-7208862	HEK293	kidney:	embryo
27	chr8:7078402-7078452	AG09319	gingival:	n/a
28	chr8:7191273-7191323	HEK293	kidney:	embryo
29	chr8:7192145-7192195	T-47D	breast:	n/a
30	chr8:7189580-7189630	A549	lung:	n/a
31	chr8:7153685-7153735	Caco-2	colon:	n/a
32	chr8:7079761-7079811	AG09319	gingival:	n/a
33	chr8:7151550-7151600	SAEC	small airway:	n/a
34	chr8:7189580-7189630	GM12878	blood:	n/a
35	chr8:7015931-7015981	GM06990	blood:	n/a
36	chr8:7004819-7004869	AG04449	skin:	fetal
37	chr8:7144084-7144134	SAEC	small airway:	n/a
38	chr8:7192145-7192195	U87	brain:	n/a
39	chr8:7144084-7144134	SK-N-SH_RA	brain:	n/a
40	chr8:7015931-7015981	SK-N-SH	brain:	n/a
41	chr8:7076476-7076526	BE2_C	brain:	n/a
42	chr8:7079037-7079087	NB4	blood:	n/a
43	chr8:7191273-7191323	PFSK-1	brain:	n/a
44	chr8:7079037-7079087	AG09319	gingival:	n/a
45	chr8:7120562-7120612	SAEC	small airway:	n/a
46	chr8:7189580-7189630	ovcar-3	ovarian:	n/a
47	chr8:7076476-7076526	AG09319	gingival:	n/a
48	chr8:7212941-7212991	RPTEC	kidney:	n/a
49	chr8:7113462-7113512	BE2_C	brain:	n/a
50	chr8:7157397-7157447	RPTEC	kidney:	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	chr8:7206593-7206668	NONHSAT124826
2	lnc-ZNF705G-1	chr8:7181819-7181886	NONHSAT124824
3	lnc-ZNF705G-1	chr8:7206605-7206668	NONHSAT124824
4	lnc-ZNF705G-1	chr8:7182344-7182411	NONHSAT124824
5	lnc-DEFB105B-3	chr8:7177268-7177473	NONHSAT124823
6	lnc-ZNF705G-1	chr8:7212333-7212574	NONHSAT124826
7	lnc-ZNF705G-1	chr8:7182659-7182720	NONHSAT124824
8	lnc-ZNF705G-1	chr8:7180835-7180882	NONHSAT124824
9	lnc-DEFB105B-4	chr8:7010239-7010328	NONHSAT124814
10	lnc-DEFB105B-4	chr8:7043806-7044422	NONHSAT124814
11	lnc-DEFA5-2	chr8:7001154-7001363	NONHSAT124813
12	lnc-DEFB105B-3	chr8:7170368-7170425	NONHSAT124823
13	lnc-ZNF705G-1	chr8:7212333-7212511	NONHSAT124824

No data

Variant related genes	Relation type
DEFB108P2	TF binding region
ENSG00000254683	TF binding region
FAM90A13P	TF binding region
FAM90A5P	TF binding region
ENSG00000216206	TF binding region
ENSG00000234120	TF binding region
ZNF705G	TF binding region
FAM90A20P	TF binding region
DEFB109P1B	TF binding region
ENSG00000231930	TF binding region
ENSG00000235778	TF binding region
OR7E125P	TF binding region
ENSG00000221567	TF binding region
ENSG00000230106	TF binding region
FAM66B	TF binding region
RPS3AP30	TF binding region
ENSG00000255025	TF binding region
FAM90A3P	TF binding region
RPS3AP33	TF binding region
USP17L1P	TF binding region
USP17L4	TF binding region
FAM90A4P	TF binding region
FAM90A15P	TF binding region
DEFB108P2	CpG island
ENSG00000254683	CpG island
FAM90A13P	CpG island
FAM90A5P	CpG island
ENSG00000216206	CpG island
ENSG00000234120	CpG island
ZNF705G	CpG island
FAM90A20P	CpG island
DEFB109P1B	CpG island
ENSG00000231930	CpG island
ENSG00000235778	CpG island
OR7E125P	CpG island
ENSG00000221567	CpG island
ENSG00000230106	CpG island
FAM66B	CpG island
RPS3AP30	CpG island
ENSG00000255025	CpG island
FAM90A3P	CpG island
RPS3AP33	CpG island
USP17L1P	CpG island
USP17L4	CpG island
FAM90A4P	CpG island
FAM90A15P	CpG island
ENSG00000226711	chromatin interactions

Extended variants
information (count: 4464 )
Associated
traits (count: 153 )

Variant overlapped rSNPs/rCNVs (count:4464 , 50 per page) page: 1 2 3 4 5 6 7 ... 90

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs555953033	chr8:6959830-6959831	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs566315565	chr8:6959839-6959840	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs535329718	chr8:6959859-6959860	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs558515632	chr8:6959871-6959872	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs577940154	chr8:6959908-6959909	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs543764317	chr8:6959910-6959911	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs545143874	chr8:6959951-6959952	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs202166364	chr8:6959954-6959955	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs368564703	chr8:6959972-6959973	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs557098160	chr8:6959976-6959977	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs574031403	chr8:6959983-6959984	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs9694864	chr8:6960003-6960004	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs561536750	chr8:6960004-6960005	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs527531072	chr8:6960015-6960016	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs374914421	chr8:6960022-6960023	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs540905807	chr8:6960050-6960051	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs564440454	chr8:6960056-6960057	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs533094907	chr8:6960080-6960081	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs549724244	chr8:6960105-6960106	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs62486914	chr8:6960111-6960112	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs62486915	chr8:6960113-6960114	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs549144052	chr8:6960124-6960125	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs566252584	chr8:6960135-6960136	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs535264952	chr8:6960137-6960138	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs558398696	chr8:6960139-6960140	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs571880596	chr8:6960141-6960142	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs537347489	chr8:6960158-6960159	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs557282602	chr8:6960166-6960167	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs572149985	chr8:6960171-6960172	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs573990637	chr8:6960175-6960176	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs542709293	chr8:6960179-6960180	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs553080192	chr8:6960189-6960190	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs540700790	chr8:6960193-6960194	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs537858893	chr8:6960201-6960202	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs78752843	chr8:6960204-6960205	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs376214480	chr8:6960205-6960206	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs115177674	chr8:6960218-6960219	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs200433424	chr8:6960221-6960222	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs116684810	chr8:6960224-6960225	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs543364214	chr8:6960228-6960229	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs563289879	chr8:6960271-6960272	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs188543548	chr8:6960290-6960291	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs369466139	chr8:6960291-6960292	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs10094923	chr8:6960310-6960311	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs181684811	chr8:6960317-6960318	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs551903847	chr8:6960319-6960320	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs571756801	chr8:6960323-6960324	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs185805611	chr8:6960349-6960350	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs150919677	chr8:6960354-6960355	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs529607163	chr8:6960375-6960376	Weak transcription	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
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Williams Syndrome	20824207	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:301 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:6958000-6961400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr8:6959600-6969000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr8:6960800-6962000	Enhancers	iPS-20b Cell Line	embryonic stem cell
4	chr8:6961200-6962200	Enhancers	HUES6 Cell Line	embryonic stem cell
5	chr8:6961400-6961800	Enhancers	iPS-15b Cell Line	embryonic stem cell
6	chr8:6961400-6962200	Enhancers	H1 Cell Line	embryonic stem cell
7	chr8:6961400-6962200	Enhancers	iPS-18 Cell Line	embryonic stem cell
8	chr8:6961400-6962400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr8:6961400-6962400	Enhancers	HUES48 Cell Line	embryonic stem cell
10	chr8:6961800-6962200	Enhancers	HUES64 Cell Line	embryonic stem cell
11	chr8:6961800-6962800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
12	chr8:6962000-6962400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
13	chr8:6962800-6963000	Enhancers	iPS-15b Cell Line	embryonic stem cell
14	chr8:6966400-6966800	Enhancers	ES-I3 Cell Line	embryonic stem cell
15	chr8:6966400-6967000	Enhancers	iPS-15b Cell Line	embryonic stem cell
16	chr8:6967400-6968400	Enhancers	Primary neutrophils fromperipheralblood	blood
17	chr8:6969000-6969200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr8:6985000-6985400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr8:6995000-6995600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
20	chr8:6995600-6996400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
21	chr8:6997000-7002200	Weak transcription	Dnd41	blood
22	chr8:6998600-6998800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
23	chr8:7001600-7004800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
24	chr8:7002200-7005000	Strong transcription	Dnd41	blood
25	chr8:7004800-7005000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
26	chr8:7005000-7011600	Weak transcription	Dnd41	blood
27	chr8:7006000-7011400	Weak transcription	HUES6 Cell Line	embryonic stem cell
28	chr8:7008800-7009200	Enhancers	Fetal Heart	heart
29	chr8:7009200-7010200	Weak transcription	Fetal Heart	heart
30	chr8:7009200-7011600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
31	chr8:7009800-7010400	Enhancers	H9 Cell Line	embryonic stem cell
32	chr8:7010200-7010400	Weak transcription	HUES64 Cell Line	embryonic stem cell
33	chr8:7010200-7010400	Enhancers	iPS-18 Cell Line	embryonic stem cell
34	chr8:7010400-7010600	Enhancers	HUES48 Cell Line	embryonic stem cell
35	chr8:7010400-7010600	Enhancers	HUES64 Cell Line	embryonic stem cell
36	chr8:7010400-7010600	Enhancers	iPS-15b Cell Line	embryonic stem cell
37	chr8:7010400-7010600	Enhancers	Fetal Heart	heart
38	chr8:7010400-7014600	Weak transcription	H9 Cell Line	embryonic stem cell
39	chr8:7010400-7014600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
40	chr8:7010600-7011600	Weak transcription	HUES48 Cell Line	embryonic stem cell
41	chr8:7010600-7014600	Weak transcription	HUES64 Cell Line	embryonic stem cell
42	chr8:7010600-7014600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
43	chr8:7011200-7013400	Weak transcription	H1 Cell Line	embryonic stem cell
44	chr8:7011400-7012600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr8:7011400-7012600	Strong transcription	HUES6 Cell Line	embryonic stem cell
46	chr8:7011600-7012200	Strong transcription	iPS-20b Cell Line	embryonic stem cell
47	chr8:7011600-7012400	Strong transcription	HUES48 Cell Line	embryonic stem cell
48	chr8:7011600-7012400	Strong transcription	Dnd41	blood
49	chr8:7012200-7014600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
50	chr8:7012400-7012600	Enhancers	ES-I3 Cell Line	embryonic stem cell

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