Variant report

Variant	nsv465468
Chromosome Location	chr8:11818364-11898209
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	ARID3A	chr8:11872669-11872691	HepG2	liver:	n/a	n/a
2	BATF	chr8:11895971-11896326	GM12878	blood:	n/a	n/a
3	BCL3	chr8:11822405-11822652	GM12878	blood:	n/a	n/a
4	CBX3	chr8:11839401-11840135	HCT-116	colon:	n/a	n/a
5	CCNT2	chr8:11872580-11872794	K562	blood:	n/a	n/a
6	CCNT2	chr8:11843856-11844050	K562	blood:	n/a	n/a
7	CEBPB	chr8:11852501-11853120	HCT-116	colon:	n/a	chr8:11852980-11852993
8	CEBPB	chr8:11858243-11858418	HepG2	liver:	n/a	n/a
9	CEBPB	chr8:11854282-11854495	HepG2	liver:	n/a	chr8:11854359-11854368 chr8:11854357-11854368 chr8:11854359-11854370
10	CEBPB	chr8:11858214-11858354	IMR90	lung:	n/a	n/a
11	CEBPB	chr8:11821309-11821507	HepG2	liver:	n/a	chr8:11821395-11821406
12	CEBPB	chr8:11854194-11854540	K562	blood:	n/a	chr8:11854359-11854368 chr8:11854357-11854368 chr8:11854359-11854370
13	CEBPB	chr8:11854319-11854398	H1-hESC	embryonic stem cell:	n/a	chr8:11854359-11854368 chr8:11854357-11854368 chr8:11854359-11854370
14	CEBPB	chr8:11854216-11854508	IMR90	lung:	n/a	chr8:11854359-11854368 chr8:11854357-11854368 chr8:11854359-11854370
15	CEBPB	chr8:11858214-11858439	A549	lung:	n/a	n/a
16	CEBPB	chr8:11852658-11853061	IMR90	lung:	n/a	chr8:11852980-11852993
17	CHD2	chr8:11844195-11844527	H1-hESC	embryonic stem cell:	n/a	n/a
18	CHD2	chr8:11832848-11832898	K562	blood:	n/a	n/a
19	CTCF	chr8:11872621-11872890	Hela-S3	cervix:	n/a	chr8:11872722-11872738 chr8:11872721-11872739
20	CTCF	chr8:11828100-11828250	HEK293	kidney:	n/a	chr8:11828185-11828201
21	CTCF	chr8:11827861-11827883	GM10266	blood:	n/a	n/a
22	CTCF	chr8:11872660-11872810	RPTEC	kidney:	n/a	chr8:11872722-11872738 chr8:11872721-11872739
23	CTCF	chr8:11828120-11828270	RPTEC	kidney:	n/a	chr8:11828185-11828201
24	CTCF	chr8:11828077-11828308	K562	blood:	n/a	chr8:11828185-11828201
25	CTCF	chr8:11828140-11828290	K562	blood:	n/a	chr8:11828185-11828201
26	CTCF	chr8:11828100-11828320	GM19239	blood:	n/a	chr8:11828185-11828201
27	CTCF	chr8:11828135-11828232	Medullo	brain:	n/a	chr8:11828185-11828201
28	CTCF	chr8:11872740-11872890	HRPEpiC	eye:	n/a	n/a
29	CTCF	chr8:11823660-11823810	GM12871	blood:	n/a	n/a
30	CTCF	chr8:11872680-11872830	GM12865	blood:	n/a	chr8:11872722-11872738 chr8:11872721-11872739
31	CTCF	chr8:11828550-11828776	K562	blood:	n/a	n/a
32	CTCF	chr8:11872760-11872910	HPF	lung:	n/a	n/a
33	CTCF	chr8:11872640-11872790	NHEK	skin:	n/a	chr8:11872722-11872738 chr8:11872721-11872739
34	CTCF	chr8:11828074-11828292	ProgFib	skin:	n/a	chr8:11828185-11828201
35	CTCF	chr8:11844120-11844270	SK-N-SH_RA	brain:	n/a	n/a
36	CTCF	chr8:11839680-11839830	HCFaa	heart:	n/a	n/a
37	CTCF	chr8:11872612-11872899	GM10266	blood:	n/a	chr8:11872722-11872738 chr8:11872721-11872739
38	CTCF	chr8:11872583-11872907	GM12892	blood:	n/a	chr8:11872722-11872738 chr8:11872721-11872739
39	CTCF	chr8:11828440-11828590	WI-38	lung:	n/a	n/a
40	CTCF	chr8:11820125-11820432	MCF-7	breast:	n/a	n/a
41	CTCF	chr8:11844000-11844150	HRPEpiC	eye:	n/a	n/a
42	CTCF	chr8:11828596-11828856	GM12878	blood:	n/a	n/a
43	CTCF	chr8:11828008-11828382	GM12878	blood:	n/a	chr8:11828185-11828201
44	CTCF	chr8:11828120-11828270	Hela-S3	cervix:	n/a	chr8:11828185-11828201
45	CTCF	chr8:11828042-11828237	SK-N-SH_RA	brain:	n/a	chr8:11828185-11828201
46	CTCF	chr8:11872660-11872810	NHDF-neo	bronchial:	n/a	chr8:11872722-11872738 chr8:11872721-11872739
47	CTCF	chr8:11828120-11828270	SAEC	small airway:	n/a	chr8:11828185-11828201
48	CTCF	chr8:11872700-11872850	GM12864	blood:	n/a	chr8:11872722-11872738 chr8:11872721-11872739
49	CTCF	chr8:11828549-11828881	K562	blood:	n/a	n/a
50	CTCF	chr8:11828580-11828730	SAEC	small airway:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:11839780-11839830	SK-N-MC	brain:	n/a
2	chr8:11872659-11872709	PrEC	prostate:	n/a
3	chr8:11838532-11838582	AG10803	skin:	n/a
4	chr8:11839780-11839830	SK-N-MC	brain:	n/a
5	chr8:11872659-11872709	PrEC	prostate:	n/a
6	chr8:11838532-11838582	AG10803	skin:	n/a
7	chr8:11872778-11872828	A549	lung:	n/a
8	chr8:11872882-11872932	AG04450	lung:	fetal
9	chr8:11843816-11843866	SK-N-SH_RA	brain:	n/a
10	chr8:11835607-11835657	HMEC	breast:	n/a
11	chr8:11843807-11843857	NHBE	bronchial:	n/a
12	chr8:11839780-11839830	U87	brain:	n/a
13	chr8:11839138-11839188	MCF-7	breast:	n/a
14	chr8:11872141-11872191	HEEpiC	esophagus:	n/a
15	chr8:11843971-11844021	AG04450	lung:	fetal
16	chr8:11831823-11831873	BJ	skin:	n/a
17	chr8:11831823-11831873	HCM	heart:	n/a
18	chr8:11872659-11872709	SK-N-MC	brain:	n/a
19	chr8:11839138-11839188	SAEC	small airway:	n/a
20	chr8:11872778-11872828	GM19239	blood:	n/a
21	chr8:11872778-11872828	AG04450	lung:	fetal
22	chr8:11872141-11872191	HCF	heart:	n/a
23	chr8:11872659-11872709	PFSK-1	brain:	n/a
24	chr8:11882962-11883012	GM12891	blood:	n/a
25	chr8:11870338-11870388	ECC-1	luminal epithelium:	n/a
26	chr8:11882982-11883032	SK-N-SH_RA	brain:	n/a
27	chr8:11838843-11838893	AG04450	lung:	fetal
28	chr8:11853878-11853928	PANC-1	pancreas:	n/a
29	chr8:11833191-11833241	NT2-D1	testis:	n/a
30	chr8:11839780-11839830	A549	lung:	n/a
31	chr8:11853878-11853928	ovcar-3	ovarian:	n/a
32	chr8:11835607-11835657	GM12891	blood:	n/a
33	chr8:11882897-11882947	ovcar-3	ovarian:	n/a
34	chr8:11835607-11835657	SK-N-SH	brain:	n/a
35	chr8:11839138-11839188	AoSMC	blood vessel:	n/a
36	chr8:11833191-11833241	GM06990	blood:	n/a
37	chr8:11895252-11895302	NT2-D1	testis:	n/a
38	chr8:11833039-11833089	NHBE	bronchial:	n/a
39	chr8:11833191-11833241	SK-N-SH	brain:	n/a
40	chr8:11833191-11833241	HEK293	kidney:	embryo
41	chr8:11872778-11872828	HUVEC	blood vessel:	n/a
42	chr8:11872141-11872191	MCF10A-Er-Src	breast:	n/a
43	chr8:11841980-11842030	GM12878	blood:	n/a
44	chr8:11882897-11882947	HepG2	liver:	n/a
45	chr8:11882982-11883032	SKMC	muscle:	n/a
46	chr8:11832261-11832311	SK-N-SH_RA	brain:	n/a
47	chr8:11872141-11872191	Caco-2	colon:	n/a
48	chr8:11853920-11853970	ProgFib	skin:	n/a
49	chr8:11839764-11839814	HCPEpiC	choroid plexus:	n/a
50	chr8:11882897-11882947	SK-N-MC	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:64863606..64864139-chr8:11882400..11882963,2	Hela-S3	cervix:
2	chr8:11816060..11816951-chr8:11827752..11828579,2	MCF-7	breast:
3	chr8:11835676..11838476-chr8:11840654..11843385,2	K562	blood:
4	chr8:11835676..11838476-chr8:11840654..11843385,2	K562	blood:
5	chr8:11833455..11835537-chr8:11843531..11845955,2	K562	blood:
6	chr8:11830756..11832686-chr8:11834027..11835713,2	K562	blood:
7	chr8:11820183..11822422-chr8:11827376..11829261,2	K562	blood:
8	chr8:11838617..11840884-chr8:11844089..11846019,2	K562	blood:
9	chr8:11820183..11822422-chr8:11827376..11829261,2	K562	blood:
10	chr8:11819737..11820672-chr8:11872272..11872975,3	MCF-7	breast:
11	chr8:11835676..11837241-chr8:11840654..11843342,2	K562	blood:
12	chr8:11836841..11840054-chr8:11842955..11845395,3	MCF-7	breast:
13	chr8:11819737..11820672-chr8:11872272..11872975,3	MCF-7	breast:
14	chr8:11827300..11830194-chr8:11832454..11834607,2	K562	blood:
15	chr8:11833455..11835537-chr8:11843531..11845955,2	K562	blood:
16	chr8:11816131..11817071-chr8:11827985..11828641,3	K562	blood:
17	chr8:11827300..11830194-chr8:11832454..11834607,2	K562	blood:
18	chr8:11835676..11837241-chr8:11840654..11843342,2	K562	blood:
19	chr8:11851923..11853652-chr8:11853797..11856578,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DEFB134-1	chr8:11860909-11861591	NONHSAT125106
2	lnc-DEFB135-1	chr8:11856596-11856977	NONHSAT125105

Variant related genes	Relation type
DEFB136	TF binding region
ENSG00000255016	TF binding region
ENSG00000255174	TF binding region
DEFB134	TF binding region
ENSG00000254507	TF binding region
DEFB135	TF binding region
ENSG00000255098	TF binding region
OR7E160P	TF binding region
DEFB136	CpG island
ENSG00000255016	CpG island
ENSG00000255174	CpG island
DEFB134	CpG island
ENSG00000254507	CpG island
DEFB135	CpG island
ENSG00000255098	CpG island
OR7E160P	CpG island
ENSG00000205883	chromatin interactions
ENSG00000205884	chromatin interactions
ENSG00000149823	chromatin interactions
ENSG00000205882	chromatin interactions

Extended variants
information (count: 3432 )
Associated
traits (count: 144 )

Variant overlapped rSNPs/rCNVs (count:3432 , 50 per page) page: 1 2 3 4 5 6 7 ... 69

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9644758	chr8:11818364-11818365	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs553863882	chr8:11818396-11818397	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs574802896	chr8:11818411-11818412	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs369313346	chr8:11818426-11818427	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs34905783	chr8:11818482-11818483	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs78202093	chr8:11818491-11818492	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs117850684	chr8:11818493-11818494	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs556178815	chr8:11818513-11818514	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs150563181	chr8:11818549-11818550	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs564417584	chr8:11818578-11818579	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs530450394	chr8:11818588-11818589	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs576341914	chr8:11818605-11818606	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs573240025	chr8:11818650-11818651	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs540277628	chr8:11818673-11818674	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs561712466	chr8:11818674-11818675	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs529563224	chr8:11818676-11818677	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs550839176	chr8:11818688-11818689	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs562783764	chr8:11818703-11818704	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs192188778	chr8:11818718-11818719	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs73536660	chr8:11818736-11818737	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs551905804	chr8:11818755-11818756	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs372477735	chr8:11818808-11818809	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs375619274	chr8:11818809-11818810	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs376827985	chr8:11818816-11818817	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs74302431	chr8:11818817-11818818	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs565408790	chr8:11818828-11818829	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs184355710	chr8:11818848-11818849	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs570463462	chr8:11818887-11818888	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs534684122	chr8:11818890-11818891	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs199509046	chr8:11818926-11818927	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs546345686	chr8:11818932-11818933	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs377061312	chr8:11818966-11818967	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs188763829	chr8:11819046-11819047	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs535784102	chr8:11819047-11819048	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs557281853	chr8:11819086-11819087	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs12545242	chr8:11819105-11819106	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs539257571	chr8:11819118-11819119	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs557890966	chr8:11819120-11819121	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs138571499	chr8:11819127-11819128	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs12550278	chr8:11819165-11819166	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs561773826	chr8:11819170-11819171	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs573681662	chr8:11819181-11819182	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs114172783	chr8:11819198-11819199	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs149327984	chr8:11819201-11819202	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs533634816	chr8:11819220-11819221	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs78491036	chr8:11819263-11819264	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs376343010	chr8:11819282-11819283	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs73536662	chr8:11819369-11819370	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs368246096	chr8:11819402-11819403	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs4624991	chr8:11819404-11819405	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance

Variant related diseases (count:144)

Disease	PMID	Source
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
Acute myeloid leukemia	21251322	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
Lung squamous cell carcinoma	22363434	CNVD
Medulloblastoma	16783165	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
Myxofibrosarcoma	16751306	CNVD
Immune disease	21572526	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Kallmann Syndrome 2	22470819	CNVD
Developmental disorder	20461109	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Glioblastoma multiforme	21138945	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Gastric cancer	21811585	CNVD
Colorectal cancer	16774939	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Cancer	20164919	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD
Osteosarcoma	21215367	CNVD
Renal cell carcinoma	21215367	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
early-passage human iPS cells	21368824	CNVD
Schizophrenia	20967226	CNVD

Chromatin state (count:641 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:11813800-11823600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr8:11813800-11824600	Weak transcription	Pancreas	Pancrea
3	chr8:11814000-11821000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
4	chr8:11814000-11821200	Weak transcription	HUES6 Cell Line	embryonic stem cell
5	chr8:11814200-11821400	Weak transcription	Rectal Smooth Muscle	rectum
6	chr8:11814400-11821200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
7	chr8:11815200-11821200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr8:11815200-11823000	Weak transcription	Monocytes-CD14+_RO01746	blood
9	chr8:11815400-11821000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr8:11815400-11821600	Weak transcription	Primary monocytes fromperipheralblood	blood
11	chr8:11816800-11821200	Weak transcription	Ovary	ovary
12	chr8:11820200-11821200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
13	chr8:11820200-11822400	Enhancers	Fetal Stomach	stomach
14	chr8:11820600-11821800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
15	chr8:11820800-11821600	Enhancers	Stomach Smooth Muscle	stomach
16	chr8:11821000-11821400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr8:11821000-11822000	Enhancers	ES-I3 Cell Line	embryonic stem cell
18	chr8:11821200-11821600	Bivalent Enhancer	Adipose Nuclei	Adipose
19	chr8:11821200-11821800	Enhancers	HUES6 Cell Line	embryonic stem cell
20	chr8:11821200-11821800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
21	chr8:11821200-11821800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr8:11821200-11821800	Enhancers	Ovary	ovary
23	chr8:11821200-11822000	Enhancers	Brain Germinal Matrix	brain
24	chr8:11821200-11822200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
25	chr8:11821200-11823800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
26	chr8:11821400-11821600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr8:11821400-11821600	Enhancers	Colon Smooth Muscle	Colon
28	chr8:11821400-11821600	Bivalent Enhancer	Fetal Muscle Leg	muscle
29	chr8:11821400-11821600	Enhancers	Rectal Smooth Muscle	rectum
30	chr8:11821400-11821800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
31	chr8:11821400-11821800	Enhancers	HUES64 Cell Line	embryonic stem cell
32	chr8:11821600-11821800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr8:11821600-11822400	Enhancers	Duodenum Smooth Muscle	Duodenum
34	chr8:11821600-11824200	Enhancers	Primary monocytes fromperipheralblood	blood
35	chr8:11821600-11824600	Weak transcription	Colon Smooth Muscle	Colon
36	chr8:11821600-11824600	Weak transcription	Stomach Smooth Muscle	stomach
37	chr8:11821800-11826200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
38	chr8:11821800-11828200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr8:11821800-11833000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
40	chr8:11821800-11834400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
41	chr8:11822400-11822800	Weak transcription	Fetal Stomach	stomach
42	chr8:11822400-11824600	Weak transcription	Duodenum Smooth Muscle	Duodenum
43	chr8:11822800-11823800	Enhancers	Fetal Stomach	stomach
44	chr8:11823000-11823600	Enhancers	Monocytes-CD14+_RO01746	blood
45	chr8:11823600-11824000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
46	chr8:11823800-11824200	Bivalent Enhancer	Fetal Stomach	stomach
47	chr8:11824000-11826200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr8:11824200-11826000	Weak transcription	Primary monocytes fromperipheralblood	blood
49	chr8:11824200-11827000	Enhancers	Fetal Stomach	stomach
50	chr8:11824600-11824800	Enhancers	Pancreas	Pancrea

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