Variant report

Variant	nsv871089
Chromosome Location	chr1:79353655-79471959
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	BHLHE40	chr1:79405513-79405527	GM12878	blood:	n/a	n/a
2	BRCA1	chr1:79415111-79415262	Hela-S3	cervix:	n/a	n/a
3	BRCA1	chr1:79459804-79459831	Hela-S3	cervix:	n/a	n/a
4	CEBPB	chr1:79379656-79380004	HepG2	liver:	n/a	n/a
5	CEBPB	chr1:79451150-79451399	K562	blood:	n/a	chr1:79451261-79451272 chr1:79451259-79451270 chr1:79451259-79451272 chr1:79451201-79451214
6	CEBPB	chr1:79409333-79409445	K562	blood:	n/a	chr1:79409399-79409408 chr1:79409398-79409409 chr1:79409397-79409408
7	CEBPB	chr1:79377662-79378457	ECC-1	luminal epithelium:	n/a	chr1:79377823-79377834 chr1:79377848-79377859 chr1:79377824-79377833 chr1:79377822-79377835 chr1:79377822-79377833
8	CEBPB	chr1:79377650-79378354	IMR90	lung:	n/a	chr1:79377823-79377834 chr1:79377848-79377859 chr1:79377824-79377833 chr1:79377822-79377835 chr1:79377822-79377833
9	CEBPB	chr1:79451090-79451446	IMR90	lung:	n/a	chr1:79451261-79451272 chr1:79451259-79451270 chr1:79451259-79451272 chr1:79451201-79451214
10	CEBPB	chr1:79379712-79379997	A549	lung:	n/a	n/a
11	CEBPB	chr1:79377650-79378354	HepG2	liver:	n/a	chr1:79377823-79377834 chr1:79377848-79377859 chr1:79377824-79377833 chr1:79377822-79377835 chr1:79377822-79377833
12	CEBPB	chr1:79377703-79378070	A549	lung:	n/a	chr1:79377823-79377834 chr1:79377848-79377859 chr1:79377824-79377833 chr1:79377822-79377835 chr1:79377822-79377833
13	CEBPB	chr1:79377613-79378467	Hela-S3	cervix:	n/a	chr1:79377823-79377834 chr1:79377848-79377859 chr1:79377824-79377833 chr1:79377822-79377835 chr1:79377822-79377833
14	CEBPB	chr1:79451113-79451392	HepG2	liver:	n/a	chr1:79451261-79451272 chr1:79451259-79451270 chr1:79451259-79451272 chr1:79451201-79451214
15	CEBPB	chr1:79379650-79380020	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr1:79377671-79378334	A549	lung:	n/a	chr1:79377823-79377834 chr1:79377848-79377859 chr1:79377824-79377833 chr1:79377822-79377835 chr1:79377822-79377833
17	CEBPB	chr1:79377749-79377922	H1-hESC	embryonic stem cell:	n/a	chr1:79377823-79377834 chr1:79377848-79377859 chr1:79377824-79377833 chr1:79377822-79377835 chr1:79377822-79377833
18	CEBPB	chr1:79470706-79470922	Hela-S3	cervix:	n/a	chr1:79470789-79470800
19	CEBPB	chr1:79409235-79409568	Hela-S3	cervix:	n/a	chr1:79409399-79409408 chr1:79409398-79409409 chr1:79409397-79409408
20	CEBPB	chr1:79409261-79409575	HepG2	liver:	n/a	chr1:79409399-79409408 chr1:79409398-79409409 chr1:79409397-79409408
21	CEBPB	chr1:79409304-79409537	IMR90	lung:	n/a	chr1:79409399-79409408 chr1:79409398-79409409 chr1:79409397-79409408
22	CEBPB	chr1:79470648-79470928	HepG2	liver:	n/a	chr1:79470789-79470800
23	CEBPB	chr1:79409258-79409472	A549	lung:	n/a	chr1:79409399-79409408 chr1:79409398-79409409 chr1:79409397-79409408
24	CEBPB	chr1:79357942-79358268	IMR90	lung:	n/a	n/a
25	CEBPB	chr1:79453639-79453775	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPB	chr1:79379678-79379999	IMR90	lung:	n/a	n/a
27	CEBPB	chr1:79379745-79379945	H1-hESC	embryonic stem cell:	n/a	n/a
28	CEBPB	chr1:79379779-79379879	K562	blood:	n/a	n/a
29	CEBPB	chr1:79405681-79405919	HepG2	liver:	n/a	n/a
30	CEBPB	chr1:79377641-79378427	ECC-1	luminal epithelium:	n/a	chr1:79377823-79377834 chr1:79377848-79377859 chr1:79377824-79377833 chr1:79377822-79377835 chr1:79377822-79377833
31	CEBPB	chr1:79414781-79415272	Hela-S3	cervix:	n/a	chr1:79414944-79414957 chr1:79414973-79414990
32	CEBPB	chr1:79414890-79415047	HepG2	liver:	n/a	chr1:79414944-79414957 chr1:79414973-79414990
33	CEBPB	chr1:79357252-79357448	H1-hESC	embryonic stem cell:	n/a	n/a
34	CEBPB	chr1:79470712-79470946	A549	lung:	n/a	chr1:79470789-79470800
35	CEBPB	chr1:79451152-79451394	A549	lung:	n/a	chr1:79451261-79451272 chr1:79451259-79451270 chr1:79451259-79451272 chr1:79451201-79451214
36	CEBPB	chr1:79378071-79378234	K562	blood:	n/a	n/a
37	CTCF	chr1:79362002-79362025	GM20000	blood:	n/a	n/a
38	CTCF	chr1:79465180-79465330	GM06990	blood:	n/a	n/a
39	CTCF	chr1:79365110-79365176	GM13976	blood:	n/a	n/a
40	CTCF	chr1:79438660-79438692	Lung_OC	lung:	n/a	n/a
41	CTCF	chr1:79363160-79363310	NHDF-neo	bronchial:	n/a	n/a
42	CTCF	chr1:79424140-79424290	NHLF	lung:	n/a	n/a
43	CTCF	chr1:79365460-79365610	GM12865	blood:	n/a	n/a
44	CTCF	chr1:79433023-79433073	GM13976	blood:	n/a	n/a
45	CTCF	chr1:79429600-79429750	GM06990	blood:	n/a	n/a
46	E2F4	chr1:79383372-79383499	MCF10A-Er-Src	breast:	n/a	n/a
47	E2F4	chr1:79368083-79368213	MCF10A-Er-Src	breast:	n/a	n/a
48	E2F4	chr1:79409879-79410355	MCF10A-Er-Src	breast:	n/a	n/a
49	E2F4	chr1:79383918-79384144	MCF10A-Er-Src	breast:	n/a	n/a
50	EP300	chr1:79377628-79378045	Hela-S3	cervix:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:79410821..79413576-chr1:79414533..79416679,2	K562	blood:
2	chr1:79356582..79358429-chr1:79361774..79364231,2	MCF-7	breast:
3	chr1:79410821..79413576-chr1:79414533..79416679,2	K562	blood:
4	chr1:79411840..79414575-chr1:79858123..79860401,2	K562	blood:
5	chr1:79370114..79372345-chr1:79443530..79445892,2	K562	blood:
6	chr1:79370114..79372345-chr1:79443530..79445892,2	K562	blood:
7	chr1:79356582..79358429-chr1:79361774..79364231,2	MCF-7	breast:

Variant related genes	Relation type
ELTD1	TF binding region

Extended variants
information (count: 4676 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:4676 , 50 per page) page: 1 2 3 4 5 6 7 ... 94

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1261980	chr1:79353655-79353656	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs149822890	chr1:79353718-79353719	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs187200904	chr1:79353723-79353724	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs192123728	chr1:79353725-79353726	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs116396536	chr1:79353744-79353745	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs116366082	chr1:79353811-79353812	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs564199585	chr1:79353841-79353842	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs576437229	chr1:79353894-79353895	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs543418508	chr1:79353950-79353951	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs182808773	chr1:79353967-79353968	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs372764842	chr1:79353989-79353990	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs568186802	chr1:79354052-79354053	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs373541845	chr1:79354067-79354068	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs10518590	chr1:79354088-79354089	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs559401997	chr1:79354089-79354090	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs185452285	chr1:79354124-79354125	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs567281710	chr1:79354128-79354129	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs570795223	chr1:79354155-79354156	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs538177393	chr1:79354192-79354193	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs549761556	chr1:79354298-79354299	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs190164219	chr1:79354330-79354331	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs535854433	chr1:79354376-79354377	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs376581764	chr1:79354392-79354393	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs553931704	chr1:79354400-79354401	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs370685688	chr1:79354408-79354409	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs140704603	chr1:79354415-79354416	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs557958667	chr1:79354463-79354464	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs182578925	chr1:79354465-79354466	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs554119366	chr1:79354470-79354471	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs531849218	chr1:79354502-79354503	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs549255804	chr1:79354515-79354516	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs543777125	chr1:79354574-79354575	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs561970046	chr1:79354590-79354591	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs577505722	chr1:79354642-79354643	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs76608499	chr1:79354679-79354680	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs536267639	chr1:79354686-79354687	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs145872007	chr1:79354715-79354716	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs559147592	chr1:79354749-79354750	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs2635120	chr1:79354844-79354845	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs377330688	chr1:79354851-79354852	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs532943939	chr1:79354881-79354882	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs564386928	chr1:79354889-79354890	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs146639984	chr1:79354918-79354919	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs367897729	chr1:79354974-79354975	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs546587139	chr1:79354975-79354976	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs566498009	chr1:79354979-79354980	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs535456791	chr1:79355000-79355001	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs373584858	chr1:79355003-79355004	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs1248478	chr1:79355059-79355060	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs141173551	chr1:79355195-79355196	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:101)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Colorectal cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Astrocytoma	17934521	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	CNVD
Melanoma	17363583	CNVD
Cancer	21129771	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	20409316	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	17133270	CNVD
Type 2 diabetes	21956041	CNVD
Uveal melanoma	20484589	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Ewing''s sarcoma	17952124	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Poland''s syndrome	22110015	CNVD
Glioblastoma multiforme	22286061	CNVD
Glioblastoma multiforme	21922591	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Cancer	22429812	CNVD
Effusion lymphoma	18079361	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
small cell lung cancer	20016488	CNVD
Colorectal cancer	16774939	CNVD
Pancreatic endocrine tumor	17639061	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:266 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:79348600-79405600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr1:79350800-79358600	Strong transcription	HUVEC	blood vessel
3	chr1:79351000-79360800	Weak transcription	Left Ventricle	heart
4	chr1:79351000-79365600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr1:79351000-79367600	Weak transcription	Adipose Nuclei	Adipose
6	chr1:79351200-79355800	Weak transcription	NH-A	brain
7	chr1:79351200-79356400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr1:79351200-79356400	Weak transcription	NHDF-Ad	bronchial
9	chr1:79351200-79357400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr1:79351200-79357600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
11	chr1:79351200-79358000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
12	chr1:79351600-79354800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
13	chr1:79356400-79358200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr1:79356400-79358200	Enhancers	NHDF-Ad	bronchial
15	chr1:79357400-79357600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr1:79357600-79358000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr1:79357600-79358400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
18	chr1:79357600-79358400	Enhancers	Muscle Satellite Cultured Cells	--
19	chr1:79357600-79358600	Enhancers	Osteobl	bone
20	chr1:79357800-79358200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
21	chr1:79358000-79358200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
22	chr1:79358000-79358400	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr1:79358200-79358400	Flanking Active TSS	NHDF-Ad	bronchial
24	chr1:79358200-79358600	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr1:79358400-79358600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
26	chr1:79358400-79358600	Active TSS	NHDF-Ad	bronchial
27	chr1:79358600-79367200	Weak transcription	HUVEC	blood vessel
28	chr1:79365600-79366600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
29	chr1:79366600-79380400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
30	chr1:79367200-79368000	Strong transcription	HUVEC	blood vessel
31	chr1:79367200-79377600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr1:79368000-79368200	Weak transcription	HUVEC	blood vessel
33	chr1:79368200-79369200	Strong transcription	HUVEC	blood vessel
34	chr1:79369200-79375000	Weak transcription	HUVEC	blood vessel
35	chr1:79371600-79404200	Weak transcription	Left Ventricle	heart
36	chr1:79374000-79383600	Weak transcription	NH-A	brain
37	chr1:79375000-79383600	Strong transcription	HUVEC	blood vessel
38	chr1:79376000-79376400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
39	chr1:79376000-79376400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
40	chr1:79376000-79376800	Enhancers	Muscle Satellite Cultured Cells	--
41	chr1:79376400-79377600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr1:79376800-79382800	Weak transcription	Muscle Satellite Cultured Cells	--
43	chr1:79377400-79378200	Enhancers	Adipose Nuclei	Adipose
44	chr1:79377400-79380000	Enhancers	Primary monocytes fromperipheralblood	blood
45	chr1:79377600-79377800	Active TSS	Monocytes-CD14+_RO01746	blood
46	chr1:79377600-79378200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr1:79377600-79378400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr1:79377600-79378400	Enhancers	Hela-S3	cervix
49	chr1:79377800-79378000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
50	chr1:79377800-79378000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood

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