Variant report

Variant	nsv982153
Chromosome Location	chr8:131391067-131407495
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:154)
CpG islands
(count:61)
Chromatin interactive
region (count:5)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:154 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BHLHE40	chr8:131404982-131405108	K562	blood:	n/a	n/a
2	BHLHE40	chr8:131395301-131395332	HepG2	liver:	n/a	n/a
3	BHLHE40	chr8:131393960-131394119	K562	blood:	n/a	n/a
4	CEBPB	chr8:131394434-131394578	H1-hESC	embryonic stem cell:	n/a	n/a
5	CEBPB	chr8:131403546-131403786	HepG2	liver:	n/a	chr8:131403567-131403578 chr8:131403612-131403623
6	CEBPB	chr8:131403458-131403770	IMR90	lung:	n/a	chr8:131403567-131403578 chr8:131403612-131403623
7	CEBPB	chr8:131404886-131405088	K562	blood:	n/a	n/a
8	CEBPB	chr8:131394331-131394581	K562	blood:	n/a	n/a
9	CEBPB	chr8:131403525-131403714	K562	blood:	n/a	chr8:131403567-131403578 chr8:131403612-131403623
10	CEBPB	chr8:131403499-131403714	A549	lung:	n/a	chr8:131403567-131403578 chr8:131403612-131403623
11	CHD2	chr8:131404909-131405186	H1-hESC	embryonic stem cell:	n/a	n/a
12	CHD2	chr8:131404968-131405117	K562	blood:	n/a	n/a
13	CTCF	chr8:131392724-131392837	GM19238	blood:	n/a	n/a
14	CTCF	chr8:131402140-131402290	HAc	cerebellar:	n/a	n/a
15	CTCF	chr8:131392720-131392870	GM12869	blood:	n/a	n/a
16	CTCF	chr8:131392684-131392863	GM12892	blood:	n/a	n/a
17	CTCF	chr8:131391960-131392201	MCF-7	breast:	n/a	n/a
18	CTCF	chr8:131392740-131392890	GM12873	blood:	n/a	n/a
19	CTCF	chr8:131392038-131392138	MCF-7	breast:	n/a	n/a
20	CTCF	chr8:131392701-131392859	GM12891	blood:	n/a	n/a
21	CTCF	chr8:131392048-131392144	MCF-7	breast:	n/a	n/a
22	CTCF	chr8:131392700-131392850	K562	blood:	n/a	n/a
23	CTCF	chr8:131392660-131392810	GM12867	blood:	n/a	n/a
24	CTCF	chr8:131392723-131392840	GM19239	blood:	n/a	n/a
25	CTCF	chr8:131392700-131392850	GM12864	blood:	n/a	n/a
26	CTCF	chr8:131392700-131392850	GM12868	blood:	n/a	n/a
27	CTCF	chr8:131392718-131392861	GM12878	blood:	n/a	n/a
28	CTCF	chr8:131392680-131392830	GM12864	blood:	n/a	n/a
29	CTCF	chr8:131392700-131392850	GM12873	blood:	n/a	n/a
30	CTCF	chr8:131392031-131392113	Hela-S3	cervix:	n/a	n/a
31	CTCF	chr8:131392000-131392150	Hela-S3	cervix:	n/a	n/a
32	CTCF	chr8:131391999-131392185	MCF-7	breast:	n/a	n/a
33	CTCF	chr8:131392692-131392922	GM12878	blood:	n/a	n/a
34	CTCF	chr8:131391940-131392090	MCF-7	breast:	n/a	n/a
35	CTCF	chr8:131392060-131392210	GM12873	blood:	n/a	n/a
36	CTCF	chr8:131392707-131392841	GM19240	blood:	n/a	n/a
37	CTCF	chr8:131392660-131392810	GM12875	blood:	n/a	n/a
38	CTCF	chr8:131392680-131392830	GM12865	blood:	n/a	n/a
39	CTCF	chr8:131392760-131392910	GM12865	blood:	n/a	n/a
40	CTCF	chr8:131392711-131392879	K562	blood:	n/a	n/a
41	CTCF	chr8:131392740-131392890	GM12872	blood:	n/a	n/a
42	CTCF	chr8:131392637-131392947	K562	blood:	n/a	n/a
43	CTCF	chr8:131392060-131392210	HepG2	liver:	n/a	n/a
44	CTCF	chr8:131392717-131392838	H1-hESC	embryonic stem cell:	n/a	n/a
45	CTCF	chr8:131392720-131392870	GM12864	blood:	n/a	n/a
46	CTCF	chr8:131392640-131392790	GM06990	blood:	n/a	n/a
47	CTCF	chr8:131392000-131392150	MCF-7	breast:	n/a	n/a
48	CTCF	chr8:131392680-131392830	GM12874	blood:	n/a	n/a
49	CTCF	chr8:131392680-131392830	GM12871	blood:	n/a	n/a
50	CTCF	chr8:131392520-131392670	GM12874	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:131401332-131401382	HRPEpiC	eye:	n/a
2	chr8:131401332-131401382	HUVEC	blood vessel:	n/a
3	chr8:131401332-131401382	HEK293	kidney:	embryo
4	chr8:131401332-131401382	HL-60	blood:	n/a
5	chr8:131401332-131401382	HMEC	breast:	n/a
6	chr8:131401332-131401382	BJ	skin:	n/a
7	chr8:131401332-131401382	PANC-1	pancreas:	n/a
8	chr8:131401332-131401382	AG04450	lung:	fetal
9	chr8:131401332-131401382	ProgFib	skin:	n/a
10	chr8:131401332-131401382	IMR90	lung:	fetal
11	chr8:131401332-131401382	HAEpiC	amniotic membrane:	n/a
12	chr8:131401332-131401382	HPAEpiC	pulmonary alveolar:	n/a
13	chr8:131401332-131401382	AG09309	skin:	n/a
14	chr8:131401332-131401382	GM06990	blood:	n/a
15	chr8:131401332-131401382	NB4	blood:	n/a
16	chr8:131401332-131401382	SKMC	muscle:	n/a
17	chr8:131401332-131401382	Caco-2	colon:	n/a
18	chr8:131401332-131401382	HCT-116	colon:	n/a
19	chr8:131401332-131401382	AG10803	skin:	n/a
20	chr8:131401332-131401382	NT2-D1	testis:	n/a
21	chr8:131401332-131401382	Jurkat	blood:	n/a
22	chr8:131401332-131401382	HIPEpiC	eye:	n/a
23	chr8:131401332-131401382	HEEpiC	esophagus:	n/a
24	chr8:131401332-131401382	Hela-S3	cervix:	n/a
25	chr8:131401332-131401382	HCM	heart:	n/a
26	chr8:131401332-131401382	CMK	blood:	n/a
27	chr8:131401332-131401382	HCF	heart:	n/a
28	chr8:131401332-131401382	SK-N-MC	brain:	n/a
29	chr8:131401332-131401382	U87	brain:	n/a
30	chr8:131401332-131401382	AoSMC	blood vessel:	n/a
31	chr8:131401332-131401382	SAEC	small airway:	n/a
32	chr8:131401332-131401382	GM12878	blood:	n/a
33	chr8:131401332-131401382	HCPEpiC	choroid plexus:	n/a
34	chr8:131401332-131401382	PFSK-1	brain:	n/a
35	chr8:131401332-131401382	Hepatocyte	liver:	n/a
36	chr8:131401332-131401382	ovcar-3	ovarian:	n/a
37	chr8:131401332-131401382	T-47D	breast:	n/a
38	chr8:131401332-131401382	HNPCEpiC	eye:	n/a
39	chr8:131401332-131401382	HepG2	liver:	n/a
40	chr8:131401332-131401382	SK-N-SH_RA	brain:	n/a
41	chr8:131401332-131401382	GM12891	blood:	n/a
42	chr8:131401332-131401382	AG04449	skin:	fetal
43	chr8:131401332-131401382	A549	lung:	n/a
44	chr8:131401332-131401382	ECC-1	luminal epithelium:	n/a
45	chr8:131401332-131401382	HRCEpiC	kidney:	n/a
46	chr8:131401332-131401382	K562	blood:	n/a
47	chr8:131401332-131401382	NH-A	brain:	n/a
48	chr8:131401332-131401382	BE2_C	brain:	n/a
49	chr8:131401332-131401382	MCF-7	breast:	n/a
50	chr8:131401332-131401382	PrEC	prostate:	n/a

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:131392159..131393976-chr8:131398862..131401554,2	K562	blood:
2	chr8:131390766..131391395-chr9:126017796..126018481,2	Hela-S3	cervix:
3	chr8:131369806..131373851-chr8:131400186..131403048,3	MCF-7	breast:
4	chr8:131389274..131391733-chr8:131394975..131397039,2	K562	blood:
5	chr8:131389274..131391733-chr8:131394975..131397039,2	K562	blood:

No data

Variant related genes	Relation type
ASAP1	TF binding region
ASAP1	CpG island
ENSG00000153317	chromatin interactions

Extended variants
information (count: 690 )
Associated
traits (count: 157 )

Variant overlapped rSNPs/rCNVs (count:690 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs139713743	chr8:131391102-131391103	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs566037936	chr8:131391131-131391132	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs184627103	chr8:131391157-131391158	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs552459273	chr8:131391187-131391188	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs570749274	chr8:131391196-131391197	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs538084221	chr8:131391217-131391218	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs7822048	chr8:131391241-131391242	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs568095315	chr8:131391242-131391243	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs535496851	chr8:131391281-131391282	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs560537122	chr8:131391293-131391294	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs553508398	chr8:131391313-131391314	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs566483349	chr8:131391330-131391331	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs575230267	chr8:131391406-131391407	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs367855713	chr8:131391454-131391455	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs115170877	chr8:131391460-131391461	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs558079110	chr8:131391484-131391485	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs576308982	chr8:131391587-131391588	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs574720602	chr8:131391588-131391589	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs201159765	chr8:131391621-131391622	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs199802181	chr8:131391622-131391623	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs145249600	chr8:131391652-131391653	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs11778712	chr8:131391700-131391701	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs189810741	chr8:131391730-131391731	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs529391858	chr8:131391732-131391733	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs141237061	chr8:131391761-131391762	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs182435915	chr8:131391796-131391797	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs541466520	chr8:131391815-131391816	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs76404401	chr8:131391849-131391850	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs533405425	chr8:131391855-131391856	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs7844582	chr8:131391874-131391875	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs570785725	chr8:131391877-131391878	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs148885845	chr8:131391880-131391881	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs117974474	chr8:131391937-131391938	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs149128454	chr8:131391963-131391964	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs11784477	chr8:131391974-131391975	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs73425514	chr8:131392008-131392009	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs117615438	chr8:131392034-131392035	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs553874555	chr8:131392040-131392041	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs565637713	chr8:131392113-131392114	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs539078189	chr8:131392139-131392140	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs557315942	chr8:131392140-131392141	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs114213715	chr8:131392162-131392163	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs192191888	chr8:131392186-131392187	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs555686451	chr8:131392217-131392218	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs180959978	chr8:131392220-131392221	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs541254460	chr8:131392240-131392241	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs559844815	chr8:131392260-131392261	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs370744928	chr8:131392329-131392330	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs77303890	chr8:131392339-131392340	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs563637872	chr8:131392350-131392351	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:157)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Ewing''s sarcoma	21437220	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Gastric cancer	17908304	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Liver carcinoma	19366792	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Testicular cancer	18059402	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
abnormal development	18461090	CNVD
Oral cancer	21386901	CNVD
Uveal melanoma	21693616	CNVD
Langer-Giedion syndrome	22283845	CNVD
Cancer	21637783	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	20632083	CNVD
Breast cancer	17603634	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	19627613	CNVD
Prostate cancer	21088497	CNVD
colon cancer	17210682	CNVD
Breast cancer	21264507	CNVD
Breast cancer	22028636	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	16751803	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Gastric cancer	17167181	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	16461572	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
head and neck squamous cell carcinoma	18028549	CNVD
Breast cancer	17001317	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute myeloid leukemia	20729466	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	21399628	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	17393978	CNVD
Burkitt''s lymphoma	18698080	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Developmental delay	21147756	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Non-small cell lung cancer	19010865	CNVD
small cell lung cancer	20016488	CNVD
Papillary thyroid cancer	17515504	CNVD
Basal cell lymphoma	17053054	CNVD
Gastric cancer	21528007	CNVD
Breast cancer	22532251	CNVD
Cervical cancer	21062161	CNVD
Cancer	21129771	CNVD
benign familial neonatal convulsions	18472482	CNVD
Breast cancer	16417655	CNVD
Astrocytoma	17387387	CNVD
Cancer	21183584	CNVD
Follicular lymphoma	20505157	CNVD
T-cell lymphomas	19863542	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	20607354	CNVD
Breast cancer	20814816	CNVD
Colorectal cancer	22486879	CNVD
Breast cancer	17908964	CNVD
Colorectal cancer	20031965	CNVD
Hepatocellular carcinoma	16750200	CNVD
Ovarian cancer	17908964	CNVD
Ovarian cancer	20031965	CNVD
Prostate cancer	20031965	CNVD
Non-small cell lung cancer	17643093	CNVD
Prostate cancer	19242612	CNVD
Colorectal cancer	16774939	CNVD
Malignant melanoma	17260012	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Acute myeloid leukemia	17268525	CNVD
Acute myeloid leukemia	18379011	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Sezary syndrome	18413736	CNVD
Breast cancer	22048815	CNVD
Colorectal cancer	16912164	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Lung adenocarcinoma	21148746	CNVD
Lung cancer	21911935	CNVD
Breast cancer	20459607	CNVD
Medulloblastoma	19270706	CNVD
Acute myeloid leukemia	19651601	CNVD
Colorectal cancer	21645411	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Colorectal cancer	19455253	CNVD
Glioblastoma multiforme	22286061	CNVD
Colorectal cancer	22860045	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Lung cancer	17925434	CNVD
Non-small cell lung cancer	21829676	CNVD
Prostate cancer	17217626	CNVD
Cancer	17160897	CNVD
Breast cancer	16497871	CNVD
Colorectal cancer	16882699	CNVD
Cystic fibrosis	19273617	CNVD
Chronic stroke	19622162	CNVD
Chordoma	18071362	CNVD
Breast cancer	17850661	CNVD
head and neck squamous cell carcinoma	16740747	CNVD
Gastric cancer	22539939	CNVD
Breast cancer	16272173	CNVD
Uveal melanoma	20484589	CNVD
Ovarian cancer	20844748	CNVD
Multiple myeloma	16616336	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21611746	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Prostate cancer	22341455	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD
Gastrointestinal stromal cancer	20818650	CNVD

Chromatin state (count:471 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:131371400-131391400	Weak transcription	Spleen	Spleen
2	chr8:131371600-131419800	Weak transcription	Aorta	Aorta
3	chr8:131371800-131396400	Weak transcription	HepG2	liver
4	chr8:131371800-131398400	Weak transcription	Fetal Lung	lung
5	chr8:131374600-131409000	Weak transcription	Fetal Brain Female	brain
6	chr8:131381000-131401400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr8:131381400-131400000	Weak transcription	HUES48 Cell Line	embryonic stem cell
8	chr8:131382600-131398800	Weak transcription	Lung	lung
9	chr8:131383200-131392000	Weak transcription	Fetal Muscle Trunk	muscle
10	chr8:131383200-131396600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr8:131383200-131397600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
12	chr8:131383800-131393200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr8:131383800-131409200	Weak transcription	Right Atrium	heart
14	chr8:131384000-131400800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr8:131384600-131397000	Weak transcription	Ovary	ovary
16	chr8:131384800-131408200	Weak transcription	Adipose Nuclei	Adipose
17	chr8:131384800-131408800	Weak transcription	Brain Germinal Matrix	brain
18	chr8:131385000-131392000	Weak transcription	Esophagus	oesophagus
19	chr8:131385800-131408600	Weak transcription	Fetal Brain Male	brain
20	chr8:131387000-131398000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
21	chr8:131388400-131392000	Weak transcription	Placenta Amnion	Placenta Amnion
22	chr8:131388600-131391800	Weak transcription	HSMMtube	muscle
23	chr8:131388600-131392000	Weak transcription	Osteobl	bone
24	chr8:131388600-131392200	Weak transcription	Hela-S3	cervix
25	chr8:131388600-131392600	Weak transcription	Muscle Satellite Cultured Cells	--
26	chr8:131388600-131393400	Weak transcription	NH-A	brain
27	chr8:131388600-131396000	Weak transcription	Right Ventricle	heart
28	chr8:131388600-131396200	Weak transcription	HMEC	breast
29	chr8:131388600-131397000	Weak transcription	NHDF-Ad	bronchial
30	chr8:131388600-131398600	Weak transcription	H1 Cell Line	embryonic stem cell
31	chr8:131388600-131398800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
32	chr8:131388600-131400200	Weak transcription	H9 Cell Line	embryonic stem cell
33	chr8:131388600-131407200	Weak transcription	HSMM	muscle
34	chr8:131388800-131391200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
35	chr8:131388800-131392200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
36	chr8:131388800-131400400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
37	chr8:131388800-131400600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
38	chr8:131388800-131400800	Weak transcription	HUES64 Cell Line	embryonic stem cell
39	chr8:131388800-131408400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
40	chr8:131389400-131409200	Weak transcription	Pancreas	Pancrea
41	chr8:131389600-131392200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
42	chr8:131389600-131393000	Genic enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
43	chr8:131389600-131393200	Genic enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
44	chr8:131389600-131399200	Strong transcription	NHEK	skin
45	chr8:131389800-131396000	Strong transcription	Fetal Stomach	stomach
46	chr8:131390000-131393000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
47	chr8:131390000-131393000	Strong transcription	NHLF	lung
48	chr8:131390000-131400400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
49	chr8:131390200-131392000	Strong transcription	Placenta	Placenta
50	chr8:131390200-131395200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell

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