Variant report

Variant	nsv546624
Chromosome Location	chr1:79382009-79420491
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	chr1:79409333-79409445	K562	blood:	n/a	chr1:79409399-79409408 chr1:79409398-79409409 chr1:79409397-79409408
4	CEBPB	chr1:79409261-79409575	HepG2	liver:	n/a	chr1:79409399-79409408 chr1:79409398-79409409 chr1:79409397-79409408
5	CEBPB	chr1:79414781-79415272	Hela-S3	cervix:	n/a	chr1:79414944-79414957 chr1:79414973-79414990
6	CEBPB	chr1:79405681-79405919	HepG2	liver:	n/a	n/a
7	CEBPB	chr1:79409235-79409568	Hela-S3	cervix:	n/a	chr1:79409399-79409408 chr1:79409398-79409409 chr1:79409397-79409408
8	CEBPB	chr1:79409304-79409537	IMR90	lung:	n/a	chr1:79409399-79409408 chr1:79409398-79409409 chr1:79409397-79409408
9	CEBPB	chr1:79409258-79409472	A549	lung:	n/a	chr1:79409399-79409408 chr1:79409398-79409409 chr1:79409397-79409408
10	CEBPB	chr1:79414890-79415047	HepG2	liver:	n/a	chr1:79414944-79414957 chr1:79414973-79414990
11	E2F4	chr1:79383372-79383499	MCF10A-Er-Src	breast:	n/a	n/a
12	E2F4	chr1:79409879-79410355	MCF10A-Er-Src	breast:	n/a	n/a
13	E2F4	chr1:79383918-79384144	MCF10A-Er-Src	breast:	n/a	n/a
14	EP300	chr1:79414914-79415277	Hela-S3	cervix:	n/a	n/a
15	FOS	chr1:79418474-79418595	MCF10A-Er-Src	breast:	n/a	chr1:79418556-79418567 chr1:79418558-79418569 chr1:79418558-79418570 chr1:79418560-79418568
16	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
17	FOS	chr1:79383980-79384299	HUVEC	blood vessel:	n/a	chr1:79384134-79384142 chr1:79384134-79384141 chr1:79384132-79384143 chr1:79384133-79384142 chr1:79384134-79384143
18	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
19	FOS	chr1:79418400-79418657	HUVEC	blood vessel:	n/a	chr1:79418556-79418567 chr1:79418558-79418569 chr1:79418558-79418570 chr1:79418560-79418568
20	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
21	FOS	chr1:79403650-79403873	MCF10A-Er-Src	breast:	n/a	n/a
22	FOSL2	chr1:79383831-79384338	SK-N-SH	brain:	n/a	chr1:79384134-79384142 chr1:79384134-79384141 chr1:79384133-79384142 chr1:79384134-79384143
23	FOSL2	chr1:79383652-79384467	SK-N-SH	brain:	n/a	chr1:79384134-79384142 chr1:79384134-79384141 chr1:79384133-79384142 chr1:79384134-79384143
24	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
25	GATA3	chr1:79383427-79384834	SK-N-SH	brain:	n/a	chr1:79384766-79384782 chr1:79384663-79384676 chr1:79384097-79384107 chr1:79384771-79384778 chr1:79384764-79384785 chr1:79384769-79384778 chr1:79384766-79384782
26	GATA3	chr1:79383441-79384733	SK-N-SH	brain:	n/a	chr1:79384663-79384676 chr1:79384097-79384107
27	GATA3	chr1:79382591-79383089	SK-N-SH	brain:	n/a	chr1:79382956-79382972 chr1:79382954-79382975
28	GATA3	chr1:79416972-79417460	SK-N-SH	brain:	n/a	n/a
29	GATA3	chr1:79386972-79387051	SH-SY5Y	brain:	n/a	n/a
30	GATA3	chr1:79383638-79383679	SH-SY5Y	brain:	n/a	n/a
31	GATA3	chr1:79416880-79417437	SK-N-SH	brain:	n/a	n/a
32	JUN	chr1:79403872-79404028	K562	blood:	n/a	n/a
33	JUND	chr1:79383833-79384418	SK-N-SH	brain:	n/a	chr1:79384134-79384142 chr1:79384134-79384141 chr1:79384133-79384142 chr1:79384134-79384143
34	MAFF	chr1:79385614-79385748	HepG2	liver:	n/a	chr1:79385667-79385685
35	MAFK	chr1:79396730-79396773	HepG2	liver:	n/a	chr1:79396746-79396761
36	MAFK	chr1:79385607-79385735	HepG2	liver:	n/a	chr1:79385669-79385684
37	MAFK	chr1:79385595-79385823	HepG2	liver:	n/a	chr1:79385669-79385684
38	MYC	chr1:79417059-79417164	Hela-S3	cervix:	n/a	n/a
39	PBX3	chr1:79383592-79384634	SK-N-SH	brain:	n/a	n/a
40	POLR2A	chr1:79410488-79410490	MCF10A-Er-Src	breast:	n/a	n/a
41	POLR2A	chr1:79409612-79409812	MCF10A-Er-Src	breast:	n/a	n/a
42	POLR2A	chr1:79397530-79397556	MCF10A-Er-Src	breast:	n/a	n/a
43	POLR2A	chr1:79390976-79390991	MCF10A-Er-Src	breast:	n/a	n/a
44	POLR2A	chr1:79407255-79407367	MCF10A-Er-Src	breast:	n/a	n/a
45	POLR2A	chr1:79403737-79404169	SK-N-MC	brain:	n/a	n/a
46	POLR2A	chr1:79398310-79398346	MCF10A-Er-Src	breast:	n/a	n/a
47	POLR2A	chr1:79383860-79384169	MCF10A-Er-Src	breast:	n/a	n/a
48	POLR2A	chr1:79393553-79393709	MCF10A-Er-Src	breast:	n/a	n/a
49	POLR2A	chr1:79386959-79387035	HUVEC	blood vessel:	n/a	n/a
50	POLR2A	chr1:79414095-79414398	MCF10A-Er-Src	breast:	n/a	n/a

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

Variant related genes	Relation type
ELTD1	TF binding region

Extended variants
information (count: 1586 )
Associated
traits (count: 100 )

Variant overlapped rSNPs/rCNVs (count:1586 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1489400	chr1:79382009-79382010	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs539815714	chr1:79382034-79382035	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs533208155	chr1:79382062-79382063	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs184762705	chr1:79382083-79382084	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs80156808	chr1:79382091-79382092	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs530449423	chr1:79382104-79382105	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs1489399	chr1:79382108-79382109	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs77218378	chr1:79382138-79382139	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs112400664	chr1:79382141-79382142	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs535661090	chr1:79382155-79382156	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs113130437	chr1:79382308-79382309	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs77354328	chr1:79382309-79382310	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs566141649	chr1:79382362-79382363	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs540096042	chr1:79382375-79382376	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs374501473	chr1:79382383-79382384	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs529128833	chr1:79382387-79382388	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs549270379	chr1:79382389-79382390	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs570038261	chr1:79382399-79382400	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs537468428	chr1:79382445-79382446	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs555562361	chr1:79382517-79382518	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs977915	chr1:79382535-79382536	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs531430542	chr1:79382538-79382539	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs371501160	chr1:79382593-79382594	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs553093880	chr1:79382609-79382610	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs189622451	chr1:79382640-79382641	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs551444568	chr1:79382675-79382676	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs180875183	chr1:79382680-79382681	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs375819935	chr1:79382684-79382685	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs977914	chr1:79382704-79382705	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs142511347	chr1:79382729-79382730	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs147587231	chr1:79382739-79382740	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs560815574	chr1:79382806-79382807	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs567657281	chr1:79382840-79382841	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs111264505	chr1:79382865-79382866	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs546385189	chr1:79382866-79382867	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs566227842	chr1:79382872-79382873	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs977913	chr1:79382889-79382890	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs552080570	chr1:79382890-79382891	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs570396759	chr1:79382922-79382923	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs977912	chr1:79382934-79382935	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs185425013	chr1:79382950-79382951	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs567561896	chr1:79382971-79382972	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs535085723	chr1:79382975-79382976	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs553213793	chr1:79383009-79383010	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs577397031	chr1:79383010-79383011	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs189510762	chr1:79383020-79383021	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs556831384	chr1:79383040-79383041	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs571315298	chr1:79383064-79383065	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs12048990	chr1:79383100-79383101	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs116834304	chr1:79383179-79383180	Weak transcription Strong transcription Enhancers	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:70 , 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	chr1:79371600-79404200	Weak transcription	Left Ventricle	heart
3	chr1:79374000-79383600	Weak transcription	NH-A	brain
4	chr1:79375000-79383600	Strong transcription	HUVEC	blood vessel
5	chr1:79376800-79382800	Weak transcription	Muscle Satellite Cultured Cells	--
6	chr1:79378000-79385000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr1:79378200-79382200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr1:79378400-79382400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr1:79378400-79382400	Weak transcription	Hela-S3	cervix
10	chr1:79378400-79383800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr1:79381200-79382600	Enhancers	Primary monocytes fromperipheralblood	blood
12	chr1:79382000-79383800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
13	chr1:79382200-79383000	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr1:79382400-79383200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr1:79382400-79383400	Enhancers	Hela-S3	cervix
16	chr1:79382800-79383600	Enhancers	Muscle Satellite Cultured Cells	--
17	chr1:79383000-79383600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr1:79383200-79383600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
19	chr1:79383400-79383800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
20	chr1:79383400-79383800	Active TSS	Fetal Stomach	stomach
21	chr1:79383400-79383800	Flanking Active TSS	Hela-S3	cervix
22	chr1:79383600-79383800	Enhancers	NH-A	brain
23	chr1:79383600-79384000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
24	chr1:79383600-79384000	Flanking Active TSS	Muscle Satellite Cultured Cells	--
25	chr1:79383600-79384600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr1:79383600-79384800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
27	chr1:79383600-79384800	Enhancers	Osteobl	bone
28	chr1:79383600-79385400	Genic enhancers	HUVEC	blood vessel
29	chr1:79383800-79384400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
30	chr1:79383800-79384800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
31	chr1:79383800-79385000	Enhancers	Hela-S3	cervix
32	chr1:79383800-79400000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
33	chr1:79384000-79384800	Enhancers	Muscle Satellite Cultured Cells	--
34	chr1:79384400-79409000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr1:79384600-79385200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
36	chr1:79384600-79398600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
37	chr1:79384800-79385000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
38	chr1:79384800-79402200	Weak transcription	Muscle Satellite Cultured Cells	--
39	chr1:79385000-79385200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
40	chr1:79385400-79388000	Strong transcription	HUVEC	blood vessel
41	chr1:79388000-79390200	Weak transcription	HUVEC	blood vessel
42	chr1:79388600-79389000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr1:79390200-79398200	Strong transcription	HUVEC	blood vessel
44	chr1:79398200-79399600	Weak transcription	HUVEC	blood vessel
45	chr1:79398600-79398800	ZNF genes & repeats	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
46	chr1:79398800-79402400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr1:79399600-79405800	Strong transcription	HUVEC	blood vessel
48	chr1:79399600-79409200	Weak transcription	Adipose Nuclei	Adipose
49	chr1:79400000-79400200	ZNF genes & repeats	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
50	chr1:79400600-79402400	Weak transcription	Osteobl	bone

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