Variant report

Variant	nsv462128
Chromosome Location	chr1:79374579-79420491
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	CEBPB	chr1:79377650-79378354	HepG2	liver:	n/a	chr1:79377823-79377834 chr1:79377848-79377859 chr1:79377824-79377833 chr1:79377822-79377835 chr1:79377822-79377833
4	CEBPB	chr1:79377650-79378354	IMR90	lung:	n/a	chr1:79377823-79377834 chr1:79377848-79377859 chr1:79377824-79377833 chr1:79377822-79377835 chr1:79377822-79377833
5	CEBPB	chr1:79377671-79378334	A549	lung:	n/a	chr1:79377823-79377834 chr1:79377848-79377859 chr1:79377824-79377833 chr1:79377822-79377835 chr1:79377822-79377833
6	CEBPB	chr1:79409304-79409537	IMR90	lung:	n/a	chr1:79409399-79409408 chr1:79409398-79409409 chr1:79409397-79409408
7	CEBPB	chr1:79409333-79409445	K562	blood:	n/a	chr1:79409399-79409408 chr1:79409398-79409409 chr1:79409397-79409408
8	CEBPB	chr1:79409235-79409568	Hela-S3	cervix:	n/a	chr1:79409399-79409408 chr1:79409398-79409409 chr1:79409397-79409408
9	CEBPB	chr1:79379678-79379999	IMR90	lung:	n/a	n/a
10	CEBPB	chr1:79414781-79415272	Hela-S3	cervix:	n/a	chr1:79414944-79414957 chr1:79414973-79414990
11	CEBPB	chr1:79379650-79380020	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr1:79409258-79409472	A549	lung:	n/a	chr1:79409399-79409408 chr1:79409398-79409409 chr1:79409397-79409408
13	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
14	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
15	CEBPB	chr1:79379779-79379879	K562	blood:	n/a	n/a
16	CEBPB	chr1:79379745-79379945	H1-hESC	embryonic stem cell:	n/a	n/a
17	CEBPB	chr1:79414890-79415047	HepG2	liver:	n/a	chr1:79414944-79414957 chr1:79414973-79414990
18	CEBPB	chr1:79377613-79378467	Hela-S3	cervix:	n/a	chr1:79377823-79377834 chr1:79377848-79377859 chr1:79377824-79377833 chr1:79377822-79377835 chr1:79377822-79377833
19	CEBPB	chr1:79378071-79378234	K562	blood:	n/a	n/a
20	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
21	CEBPB	chr1:79379656-79380004	HepG2	liver:	n/a	n/a
22	CEBPB	chr1:79405681-79405919	HepG2	liver:	n/a	n/a
23	CEBPB	chr1:79379712-79379997	A549	lung:	n/a	n/a
24	CEBPB	chr1:79377703-79378070	A549	lung:	n/a	chr1:79377823-79377834 chr1:79377848-79377859 chr1:79377824-79377833 chr1:79377822-79377835 chr1:79377822-79377833
25	CEBPB	chr1:79409261-79409575	HepG2	liver:	n/a	chr1:79409399-79409408 chr1:79409398-79409409 chr1:79409397-79409408
26	E2F4	chr1:79383372-79383499	MCF10A-Er-Src	breast:	n/a	n/a
27	E2F4	chr1:79409879-79410355	MCF10A-Er-Src	breast:	n/a	n/a
28	E2F4	chr1:79383918-79384144	MCF10A-Er-Src	breast:	n/a	n/a
29	EP300	chr1:79377938-79378639	ECC-1	luminal epithelium:	n/a	n/a
30	EP300	chr1:79377628-79378045	Hela-S3	cervix:	n/a	n/a
31	EP300	chr1:79378162-79378596	ECC-1	luminal epithelium:	n/a	n/a
32	EP300	chr1:79414914-79415277	Hela-S3	cervix:	n/a	n/a
33	FOS	chr1:79383980-79384299	HUVEC	blood vessel:	n/a	chr1:79384134-79384142 chr1:79384134-79384141 chr1:79384132-79384143 chr1:79384133-79384142 chr1:79384134-79384143
34	FOS	chr1:79384039-79384310	MCF10A-Er-Src	breast:	n/a	chr1:79384134-79384142 chr1:79384134-79384141 chr1:79384132-79384143 chr1:79384133-79384142 chr1:79384134-79384143
35	FOS	chr1:79383963-79384255	MCF10A-Er-Src	breast:	n/a	chr1:79384134-79384142 chr1:79384134-79384141 chr1:79384132-79384143 chr1:79384133-79384142 chr1:79384134-79384143
36	FOS	chr1:79377671-79378004	MCF10A-Er-Src	breast:	n/a	chr1:79377756-79377767
37	FOS	chr1:79403650-79403873	MCF10A-Er-Src	breast:	n/a	n/a
38	FOS	chr1:79418400-79418657	HUVEC	blood vessel:	n/a	chr1:79418556-79418567 chr1:79418558-79418569 chr1:79418558-79418570 chr1:79418560-79418568
39	FOS	chr1:79377662-79377976	MCF10A-Er-Src	breast:	n/a	chr1:79377756-79377767
40	FOS	chr1:79377681-79377995	MCF10A-Er-Src	breast:	n/a	chr1:79377756-79377767
41	FOS	chr1:79383977-79384266	MCF10A-Er-Src	breast:	n/a	chr1:79384134-79384142 chr1:79384134-79384141 chr1:79384132-79384143 chr1:79384133-79384142 chr1:79384134-79384143
42	FOS	chr1:79377681-79378019	MCF10A-Er-Src	breast:	n/a	chr1:79377756-79377767
43	FOS	chr1:79418474-79418595	MCF10A-Er-Src	breast:	n/a	chr1:79418556-79418567 chr1:79418558-79418569 chr1:79418558-79418570 chr1:79418560-79418568
44	FOS	chr1:79376372-79376572	MCF10A-Er-Src	breast:	n/a	n/a
45	FOSL2	chr1:79383652-79384467	SK-N-SH	brain:	n/a	chr1:79384134-79384142 chr1:79384134-79384141 chr1:79384133-79384142 chr1:79384134-79384143
46	FOSL2	chr1:79383831-79384338	SK-N-SH	brain:	n/a	chr1:79384134-79384142 chr1:79384134-79384141 chr1:79384133-79384142 chr1:79384134-79384143
47	FOSL2	chr1:79376284-79376702	SK-N-SH	brain:	n/a	n/a
48	FOXM1	chr1:79377998-79378621	ECC-1	luminal epithelium:	n/a	n/a
49	GATA2	chr1:79415034-79415289	HUVEC	blood vessel:	n/a	chr1:79415105-79415114 chr1:79415070-79415086 chr1:79415117-79415125 chr1:79415102-79415112 chr1:79415098-79415119 chr1:79415192-79415204 chr1:79415105-79415112
50	GATA3	chr1:79382591-79383089	SK-N-SH	brain:	n/a	chr1:79382956-79382972 chr1:79382954-79382975

No.	Distal block	Cell Line	Cell type
1	chr1:79410821..79413576-chr1:79414533..79416679,2	K562	blood:
2	chr1:79410821..79413576-chr1:79414533..79416679,2	K562	blood:
3	chr1:79411840..79414575-chr1:79858123..79860401,2	K562	blood:

Variant related genes	Relation type
ELTD1	TF binding region

Extended variants
information (count: 1842 )
Associated
traits (count: 100 )

Variant overlapped rSNPs/rCNVs (count:1842 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10518591	chr1:79374579-79374580	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs554119965	chr1:79374623-79374624	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs572602547	chr1:79374697-79374698	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs187006870	chr1:79374734-79374735	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs192459136	chr1:79374747-79374748	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs180836645	chr1:79374783-79374784	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs375097728	chr1:79374818-79374819	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs138447272	chr1:79374894-79374895	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs562146340	chr1:79374918-79374919	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs370386862	chr1:79374981-79374982	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs185413203	chr1:79375025-79375026	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs76580578	chr1:79375026-79375027	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs559244459	chr1:79375053-79375054	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs533170183	chr1:79375057-79375058	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs374789315	chr1:79375115-79375116	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs551361631	chr1:79375138-79375139	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs563628699	chr1:79375205-79375206	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs189921174	chr1:79375218-79375219	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs149281061	chr1:79375226-79375227	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs143753370	chr1:79375231-79375232	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs182580227	chr1:79375269-79375270	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs75055578	chr1:79375298-79375299	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs187190647	chr1:79375312-79375313	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs79389962	chr1:79375401-79375402	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs539764223	chr1:79375441-79375442	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs558142768	chr1:79375591-79375592	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs576840653	chr1:79375628-79375629	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs545357284	chr1:79375633-79375634	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs376509859	chr1:79375751-79375752	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs61768744	chr1:79375786-79375787	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs531094569	chr1:79375798-79375799	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs1489402	chr1:79375882-79375883	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs560335319	chr1:79375883-79375884	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs375046919	chr1:79375999-79376000	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs115631405	chr1:79376025-79376026	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs191423592	chr1:79376043-79376044	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs183823810	chr1:79376054-79376055	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs369117395	chr1:79376062-79376063	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs188764330	chr1:79376095-79376096	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs193281289	chr1:79376098-79376099	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs530259361	chr1:79376112-79376113	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs184258258	chr1:79376158-79376159	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs186536760	chr1:79376170-79376171	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs116739563	chr1:79376216-79376217	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs10493617	chr1:79376305-79376306	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs377241057	chr1:79376313-79376314	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs148133201	chr1:79376316-79376317	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs571344810	chr1:79376345-79376346	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs564155723	chr1:79376354-79376355	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs539629122	chr1:79376398-79376399	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:100)

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

Chromatin state (count:90 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:79348600-79405600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr1:79366600-79380400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr1:79367200-79377600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr1:79369200-79375000	Weak transcription	HUVEC	blood vessel
5	chr1:79371600-79404200	Weak transcription	Left Ventricle	heart
6	chr1:79374000-79383600	Weak transcription	NH-A	brain
7	chr1:79375000-79383600	Strong transcription	HUVEC	blood vessel
8	chr1:79376000-79376400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr1:79376000-79376400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
10	chr1:79376000-79376800	Enhancers	Muscle Satellite Cultured Cells	--
11	chr1:79376400-79377600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr1:79376800-79382800	Weak transcription	Muscle Satellite Cultured Cells	--
13	chr1:79377400-79378200	Enhancers	Adipose Nuclei	Adipose
14	chr1:79377400-79380000	Enhancers	Primary monocytes fromperipheralblood	blood
15	chr1:79377600-79377800	Active TSS	Monocytes-CD14+_RO01746	blood
16	chr1:79377600-79378200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr1:79377600-79378400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr1:79377600-79378400	Enhancers	Hela-S3	cervix
19	chr1:79377800-79378000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
20	chr1:79377800-79378000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
21	chr1:79378000-79378400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
22	chr1:79378000-79378400	Enhancers	Monocytes-CD14+_RO01746	blood
23	chr1:79378000-79385000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
24	chr1:79378200-79382200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr1:79378400-79382400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr1:79378400-79382400	Weak transcription	Hela-S3	cervix
27	chr1:79378400-79383800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr1:79380000-79381200	Weak transcription	Primary monocytes fromperipheralblood	blood
29	chr1:79380400-79381200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
30	chr1:79381200-79382000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
31	chr1:79381200-79382600	Enhancers	Primary monocytes fromperipheralblood	blood
32	chr1:79382000-79383800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
33	chr1:79382200-79383000	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
34	chr1:79382400-79383200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chr1:79382400-79383400	Enhancers	Hela-S3	cervix
36	chr1:79382800-79383600	Enhancers	Muscle Satellite Cultured Cells	--
37	chr1:79383000-79383600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr1:79383200-79383600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
39	chr1:79383400-79383800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
40	chr1:79383400-79383800	Active TSS	Fetal Stomach	stomach
41	chr1:79383400-79383800	Flanking Active TSS	Hela-S3	cervix
42	chr1:79383600-79383800	Enhancers	NH-A	brain
43	chr1:79383600-79384000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
44	chr1:79383600-79384000	Flanking Active TSS	Muscle Satellite Cultured Cells	--
45	chr1:79383600-79384600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
46	chr1:79383600-79384800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
47	chr1:79383600-79384800	Enhancers	Osteobl	bone
48	chr1:79383600-79385400	Genic enhancers	HUVEC	blood vessel
49	chr1:79383800-79384400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr1:79383800-79384800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung

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