Variant report

Variant	nsv519941
Chromosome Location	chr8:11016889-11039816
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	chr8:11026563-11026651	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr8:11020411-11020492	K562	blood:	n/a	n/a
3	BATF	chr8:11034754-11035025	GM12878	blood:	n/a	chr8:11034880-11034891
4	BATF	chr8:11018551-11018700	GM12878	blood:	n/a	n/a
5	BCL3	chr8:11027876-11028173	GM12878	blood:	n/a	n/a
6	CEBPB	chr8:11028014-11028243	IMR90	lung:	n/a	chr8:11028140-11028151
7	CEBPB	chr8:11027105-11027329	K562	blood:	n/a	chr8:11027223-11027234
8	CEBPB	chr8:11027123-11027301	A549	lung:	n/a	chr8:11027223-11027234
9	CEBPB	chr8:11027148-11027316	HepG2	liver:	n/a	chr8:11027223-11027234
10	CEBPB	chr8:11027975-11028266	HepG2	liver:	n/a	chr8:11028140-11028151
11	CEBPB	chr8:11028120-11028158	H1-hESC	embryonic stem cell:	n/a	chr8:11028140-11028151
12	CEBPB	chr8:11027061-11027382	IMR90	lung:	n/a	chr8:11027223-11027234
13	CTCF	chr8:11022672-11022706	Lung_OC	lung:	n/a	n/a
14	CTCF	chr8:11038020-11038170	HAc	cerebellar:	n/a	n/a
15	CTCF	chr8:11032643-11032712	GM13976	blood:	n/a	n/a
16	CUX1	chr8:11019371-11019529	GM12878	blood:	n/a	n/a
17	EBF1	chr8:11028937-11029050	GM12878	blood:	n/a	n/a
18	EBF1	chr8:11018885-11019155	GM12878	blood:	n/a	n/a
19	EGR1	chr8:11028640-11028854	K562	blood:	n/a	chr8:11028771-11028781 chr8:11028765-11028787 chr8:11028770-11028783 chr8:11028770-11028783 chr8:11028771-11028780 chr8:11028772-11028781 chr8:11028771-11028782 chr8:11028771-11028781 chr8:11028769-11028783 chr8:11028771-11028782
20	EP300	chr8:11019448-11019567	GM12878	blood:	n/a	chr8:11019457-11019471 chr8:11019461-11019475
21	EP300	chr8:11019397-11019494	GM12878	blood:	n/a	chr8:11019457-11019471 chr8:11019461-11019475
22	FOS	chr8:11017515-11017714	MCF10A-Er-Src	breast:	n/a	n/a
23	FOS	chr8:11026272-11026685	MCF10A-Er-Src	breast:	n/a	chr8:11026496-11026507
24	FOS	chr8:11017487-11017729	MCF10A-Er-Src	breast:	n/a	n/a
25	FOS	chr8:11027852-11028154	MCF10A-Er-Src	breast:	n/a	n/a
26	FOS	chr8:11026291-11026671	MCF10A-Er-Src	breast:	n/a	chr8:11026496-11026507
27	FOS	chr8:11026348-11026652	MCF10A-Er-Src	breast:	n/a	chr8:11026496-11026507
28	FOS	chr8:11036590-11036760	MCF10A-Er-Src	breast:	n/a	n/a
29	FOS	chr8:11017515-11017715	MCF10A-Er-Src	breast:	n/a	n/a
30	FOS	chr8:11035683-11035802	MCF10A-Er-Src	breast:	n/a	n/a
31	FOS	chr8:11027876-11028155	MCF10A-Er-Src	breast:	n/a	n/a
32	FOS	chr8:11036605-11036669	MCF10A-Er-Src	breast:	n/a	n/a
33	FOS	chr8:11026277-11026709	HUVEC	blood vessel:	n/a	chr8:11026496-11026507
34	FOS	chr8:11027883-11028128	MCF10A-Er-Src	breast:	n/a	n/a
35	FOS	chr8:11036599-11036718	MCF10A-Er-Src	breast:	n/a	n/a
36	FOS	chr8:11026392-11026640	MCF10A-Er-Src	breast:	n/a	chr8:11026496-11026507
37	FOSL2	chr8:11026241-11026716	SK-N-SH	brain:	n/a	n/a
38	GATA2	chr8:11026150-11026382	K562	blood:	n/a	chr8:11026285-11026299
39	GATA2	chr8:11026159-11026575	HUVEC	blood vessel:	n/a	chr8:11026285-11026299
40	GATA2	chr8:11017310-11017511	SH-SY5Y	brain:	n/a	n/a
41	GATA3	chr8:11017254-11017786	SK-N-SH	brain:	n/a	n/a
42	GATA3	chr8:11017312-11017539	SH-SY5Y	brain:	n/a	n/a
43	GATA3	chr8:11027945-11028149	SH-SY5Y	brain:	n/a	n/a
44	JUND	chr8:11036519-11036756	H1-hESC	embryonic stem cell:	n/a	chr8:11036644-11036655
45	JUND	chr8:11036508-11036750	HepG2	liver:	n/a	chr8:11036644-11036655
46	JUND	chr8:11036328-11036917	SK-N-SH	brain:	n/a	chr8:11036644-11036655
47	KAP1	chr8:11034997-11035776	HEK293	kidney:	n/a	n/a
48	MAFF	chr8:11020295-11020501	HepG2	liver:	n/a	chr8:11020423-11020441
49	MAFF	chr8:11020387-11020494	K562	blood:	n/a	chr8:11020423-11020441
50	MAFK	chr8:11020312-11020560	HepG2	liver:	n/a	chr8:11020422-11020436 chr8:11020419-11020439 chr8:11020421-11020437

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:11021173-11021223	HepG2	liver:	n/a
2	chr8:11021173-11021223	NT2-D1	testis:	n/a
3	chr8:11021173-11021223	NH-A	brain:	n/a
4	chr8:11021173-11021223	ProgFib	skin:	n/a
5	chr8:11021173-11021223	AG04450	lung:	fetal
6	chr8:11021173-11021223	SAEC	small airway:	n/a
7	chr8:11021173-11021223	AoSMC	blood vessel:	n/a
8	chr8:11021173-11021223	U87	brain:	n/a
9	chr8:11021173-11021223	PFSK-1	brain:	n/a
10	chr8:11021173-11021223	BJ	skin:	n/a
11	chr8:11021173-11021223	Hepatocyte	liver:	n/a
12	chr8:11021173-11021223	A549	lung:	n/a
13	chr8:11021173-11021223	IMR90	lung:	fetal
14	chr8:11021173-11021223	HEEpiC	esophagus:	n/a
15	chr8:11021173-11021223	GM12891	blood:	n/a
16	chr8:11021173-11021223	K562	blood:	n/a
17	chr8:11021173-11021223	PANC-1	pancreas:	n/a
18	chr8:11021173-11021223	MCF-7	breast:	n/a
19	chr8:11021173-11021223	AG09319	gingival:	n/a
20	chr8:11021173-11021223	RPTEC	kidney:	n/a
21	chr8:11021173-11021223	HL-60	blood:	n/a
22	chr8:11021173-11021223	SKMC	muscle:	n/a
23	chr8:11021173-11021223	HNPCEpiC	eye:	n/a
24	chr8:11021173-11021223	GM19239	blood:	n/a
25	chr8:11021173-11021223	SK-N-SH_RA	brain:	n/a
26	chr8:11021173-11021223	HEK293	kidney:	embryo
27	chr8:11021173-11021223	GM06990	blood:	n/a
28	chr8:11021173-11021223	LNCaP	prostate:	n/a
29	chr8:11021173-11021223	NB4	blood:	n/a
30	chr8:11021173-11021223	GM12892	blood:	n/a
31	chr8:11021173-11021223	NHBE	bronchial:	n/a
32	chr8:11021173-11021223	HCM	heart:	n/a
33	chr8:11021173-11021223	T-47D	breast:	n/a
34	chr8:11021173-11021223	MCF10A-Er-Src	breast:	n/a
35	chr8:11021173-11021223	AG10803	skin:	n/a
36	chr8:11021173-11021223	HIPEpiC	eye:	n/a
37	chr8:11021173-11021223	HCT-116	colon:	n/a
38	chr8:11021173-11021223	NHDF-neo	bronchial:	n/a
39	chr8:11021173-11021223	AG04449	skin:	fetal
40	chr8:11021173-11021223	Caco-2	colon:	n/a
41	chr8:11021173-11021223	GM12878	blood:	n/a
42	chr8:11021173-11021223	Jurkat	blood:	n/a
43	chr8:11021173-11021223	HCPEpiC	choroid plexus:	n/a
44	chr8:11021173-11021223	ECC-1	luminal epithelium:	n/a
45	chr8:11021173-11021223	BE2_C	brain:	n/a
46	chr8:11021173-11021223	HPAEpiC	pulmonary alveolar:	n/a
47	chr8:11021173-11021223	HUVEC	blood vessel:	n/a
48	chr8:11021173-11021223	SK-N-SH	brain:	n/a
49	chr8:11021173-11021223	H1-hESC	embryonic stem cell:	embryo
50	chr8:11021173-11021223	PrEC	prostate:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:11020358..11021978-chr8:11037750..11039962,2	MCF-7	breast:
2	chr8:11020358..11021978-chr8:11037750..11039962,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AF131215.4.1-3	chr8:11021724-11022010	ucscGeneNc_uc010lrw_1
2	lnc-AF131215.4.1-3	chr8:11023544-11024685	ucscGeneNc_uc010lrw_1
3	lnc-AF131215.4.1-2	chr8:11018301-11019737	ucscGeneNc_uc010lrv_1

Variant related genes	Relation type
ENSG00000231965	TF binding region
ENSG00000231965	CpG island

Extended variants
information (count: 1273 )
Associated
traits (count: 138 )

Variant overlapped rSNPs/rCNVs (count:1273 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2409719	chr8:11016889-11016890	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs559758704	chr8:11016899-11016900	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs149791117	chr8:11016902-11016903	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs4473998	chr8:11016903-11016904	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs567268745	chr8:11016933-11016934	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs547300305	chr8:11016934-11016935	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs115966468	chr8:11016970-11016971	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs79369454	chr8:11016982-11016983	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs566926612	chr8:11016992-11016993	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs116375102	chr8:11016994-11016995	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs554197469	chr8:11017020-11017021	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs572430120	chr8:11017039-11017040	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs536667918	chr8:11017048-11017049	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs555012998	chr8:11017062-11017063	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs576496681	chr8:11017072-11017073	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs543975645	chr8:11017113-11017114	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs565388181	chr8:11017120-11017121	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs186117197	chr8:11017126-11017127	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs541289884	chr8:11017162-11017163	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs559626016	chr8:11017170-11017171	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs527263021	chr8:11017176-11017177	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs573063877	chr8:11017193-11017194	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs542228153	chr8:11017228-11017229	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs561020767	chr8:11017230-11017231	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs71518513	chr8:11017258-11017259	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs4446699	chr8:11017269-11017270	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs146821237	chr8:11017272-11017273	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs79131612	chr8:11017292-11017293	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs117132630	chr8:11017298-11017299	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs371009415	chr8:11017308-11017309	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs571391416	chr8:11017346-11017347	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs374399945	chr8:11017365-11017366	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs115700289	chr8:11017374-11017375	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs367986399	chr8:11017401-11017402	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs549095292	chr8:11017406-11017407	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs547664848	chr8:11017455-11017456	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs565996450	chr8:11017468-11017469	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs536633102	chr8:11017480-11017481	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs554695924	chr8:11017512-11017513	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs570132482	chr8:11017545-11017546	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs189699861	chr8:11017572-11017573	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs559020903	chr8:11017582-11017583	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs576980295	chr8:11017591-11017592	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs541251357	chr8:11017604-11017605	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs6999875	chr8:11017605-11017606	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs144642305	chr8:11017623-11017624	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs373313045	chr8:11017628-11017629	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs574825338	chr8:11017631-11017632	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs183265224	chr8:11017660-11017661	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs140656907	chr8:11017663-11017664	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:138)

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
abnormal development	18461090	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Glioblastoma multiforme	21138945	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Gastric cancer	21811585	CNVD
Colorectal cancer	16774939	CNVD
Breast cancer	22522925	CNVD
Acute lymphoblastic leukemia	21390130	CNVD

Chromatin state (count:339 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:10966400-11026200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr8:10997200-11021000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
3	chr8:10997400-11017400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
4	chr8:10999400-11021000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr8:11001600-11021000	Weak transcription	Primary T helper cells PMA-I stimulated	--
6	chr8:11002800-11022000	Weak transcription	HUES48 Cell Line	embryonic stem cell
7	chr8:11006800-11026200	Weak transcription	HSMM	muscle
8	chr8:11009200-11021000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
9	chr8:11009200-11024800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr8:11009800-11021400	Weak transcription	HUES64 Cell Line	embryonic stem cell
11	chr8:11012000-11021400	Weak transcription	Gastric	stomach
12	chr8:11012000-11022400	Weak transcription	H9 Cell Line	embryonic stem cell
13	chr8:11013200-11021000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
14	chr8:11013400-11026400	Weak transcription	Esophagus	oesophagus
15	chr8:11013600-11028800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
16	chr8:11014800-11017000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr8:11014800-11017400	Weak transcription	Fetal Intestine Large	intestine
18	chr8:11014800-11021400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr8:11015400-11021600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
20	chr8:11015600-11021200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
21	chr8:11015600-11022400	Enhancers	Primary B cells from peripheral blood	blood
22	chr8:11016000-11021800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr8:11016400-11017000	Flanking Active TSS	GM12878-XiMat	blood
24	chr8:11016600-11021400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
25	chr8:11016600-11032200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr8:11016800-11017200	Enhancers	Fetal Muscle Leg	muscle
27	chr8:11016800-11017200	Enhancers	Lung	lung
28	chr8:11016800-11017200	Enhancers	Pancreas	Pancrea
29	chr8:11016800-11017200	Enhancers	Spleen	Spleen
30	chr8:11016800-11017400	Enhancers	HSMMtube	muscle
31	chr8:11017000-11017200	Enhancers	Sigmoid Colon	Sigmoid Colon
32	chr8:11017000-11017400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
33	chr8:11017000-11017400	Enhancers	GM12878-XiMat	blood
34	chr8:11017000-11017800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr8:11017200-11021000	Weak transcription	Pancreas	Pancrea
36	chr8:11017200-11021400	Weak transcription	Spleen	Spleen
37	chr8:11017400-11017600	Flanking Active TSS	GM12878-XiMat	blood
38	chr8:11017400-11021200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
39	chr8:11017400-11025400	Weak transcription	HSMMtube	muscle
40	chr8:11017600-11018600	Enhancers	GM12878-XiMat	blood
41	chr8:11017800-11019000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr8:11018600-11019200	Flanking Active TSS	GM12878-XiMat	blood
43	chr8:11018800-11019000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
44	chr8:11018800-11019000	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
45	chr8:11018800-11019000	Enhancers	Sigmoid Colon	Sigmoid Colon
46	chr8:11019000-11020000	Weak transcription	Sigmoid Colon	Sigmoid Colon
47	chr8:11019000-11020200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
48	chr8:11019000-11021000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr8:11019000-11021000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
50	chr8:11019200-11019600	Active TSS	GM12878-XiMat	blood

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