Variant report

Variant	rs778650
Chromosome Location	chr3:160710141-160710142
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 85 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:83)

rs_ID	r²[population]
rs10513558	0.84[CEU][hapmap];0.89[EUR][1000 genomes]
rs10513560	0.89[CHD][hapmap];0.81[JPT][hapmap];0.89[ASN][1000 genomes]
rs10936216	0.89[ASN][1000 genomes]
rs11709802	0.84[CEU][hapmap];0.89[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs12496196	0.84[CEU][hapmap];0.89[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs12498008	0.84[CEU][hapmap];0.87[CHB][hapmap];0.87[JPT][hapmap];0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12635022	0.89[EUR][1000 genomes]
rs13079792	0.89[EUR][1000 genomes]
rs13086445	0.86[EUR][1000 genomes]
rs13325518	1.00[CHD][hapmap];0.87[JPT][hapmap];0.81[ASN][1000 genomes]
rs1348977	0.84[CEU][hapmap];0.81[TSI][hapmap]
rs1374786	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1447609	0.88[ASN][1000 genomes]
rs1447617	0.84[CEU][hapmap]
rs1530635	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1530636	0.89[CHD][hapmap];0.81[JPT][hapmap];0.89[ASN][1000 genomes]
rs1562465	0.81[JPT][hapmap];0.89[ASN][1000 genomes]
rs1562466	0.81[ASW][hapmap];0.84[CEU][hapmap];0.87[CHB][hapmap];1.00[CHD][hapmap];0.97[GIH][hapmap];0.87[JPT][hapmap];0.95[TSI][hapmap];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1599382	0.87[CHB][hapmap];0.87[JPT][hapmap];0.90[ASN][1000 genomes]
rs16831756	0.90[ASN][1000 genomes]
rs16831757	0.90[ASN][1000 genomes]
rs16831758	0.84[CEU][hapmap];0.87[CHB][hapmap];0.87[JPT][hapmap];0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1839020	0.86[EUR][1000 genomes]
rs1868104	0.84[CEU][hapmap];0.81[CHD][hapmap];0.94[GIH][hapmap];0.90[TSI][hapmap];0.86[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs1903422	0.90[ASN][1000 genomes]
rs1971240	0.84[CEU][hapmap];0.87[CHB][hapmap];0.87[JPT][hapmap];0.82[YRI][hapmap];0.93[AMR][1000 genomes];0.90[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2028988	0.91[ASW][hapmap];0.84[CEU][hapmap];0.81[CHD][hapmap];0.94[GIH][hapmap];0.90[TSI][hapmap];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2061580	0.87[CHB][hapmap];0.97[CHD][hapmap];0.86[GIH][hapmap];0.87[JPT][hapmap];0.90[ASN][1000 genomes]
rs2889391	0.89[ASN][1000 genomes]
rs34462546	0.88[ASN][1000 genomes]
rs4608736	0.81[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4679667	0.84[CEU][hapmap];0.85[EUR][1000 genomes]
rs4679925	0.89[EUR][1000 genomes]
rs4679927	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57009978	0.87[ASN][1000 genomes]
rs58189630	0.99[ASN][1000 genomes]
rs59483687	0.82[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs60875417	0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs62282273	0.90[ASN][1000 genomes]
rs6441334	0.84[CEU][hapmap]
rs6441336	0.84[CEU][hapmap]
rs6441342	0.86[EUR][1000 genomes]
rs6441343	0.89[EUR][1000 genomes]
rs6441344	0.89[EUR][1000 genomes]
rs6441345	0.87[CHD][hapmap];0.81[JPT][hapmap];0.89[ASN][1000 genomes]
rs6441346	0.89[ASN][1000 genomes]
rs6763532	0.89[ASN][1000 genomes]
rs6770180	0.89[ASN][1000 genomes]
rs6774203	0.87[CHD][hapmap];0.88[ASN][1000 genomes]
rs6785844	0.84[CEU][hapmap]
rs6787694	0.84[CEU][hapmap];0.87[CHB][hapmap];1.00[CHD][hapmap];0.97[GIH][hapmap];0.87[JPT][hapmap];0.95[TSI][hapmap];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6789195	0.84[CEU][hapmap];0.81[TSI][hapmap]
rs6797498	0.82[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs6798966	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6799391	0.84[CEU][hapmap]
rs6800013	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs73158255	0.90[ASN][1000 genomes]
rs7610732	0.84[CEU][hapmap];0.80[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7619552	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs7629001	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs7653744	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs778644	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs778647	0.84[CEU][hapmap];0.87[CHB][hapmap];0.87[JPT][hapmap];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs778651	0.87[CHB][hapmap];0.81[JPT][hapmap];1.00[ASN][1000 genomes]
rs778652	0.86[CHB][hapmap];0.87[JPT][hapmap];1.00[ASN][1000 genomes]
rs778655	0.85[CHB][hapmap];0.87[JPT][hapmap];1.00[ASN][1000 genomes]
rs778656	1.00[ASN][1000 genomes]
rs778658	0.97[ASN][1000 genomes]
rs778661	0.97[ASN][1000 genomes]
rs778662	1.00[ASN][1000 genomes]
rs796610	0.81[ASW][hapmap];0.84[CEU][hapmap];0.87[CHB][hapmap];0.97[CHD][hapmap];1.00[GIH][hapmap];0.87[JPT][hapmap];0.95[TSI][hapmap];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs814092	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs878954	0.90[EUR][1000 genomes]
rs878955	0.89[EUR][1000 genomes]
rs898676	0.87[CHB][hapmap];0.87[JPT][hapmap];0.88[ASN][1000 genomes]
rs898678	0.88[ASN][1000 genomes]
rs898679	0.87[ASN][1000 genomes]
rs935500	0.86[EUR][1000 genomes]
rs9814174	0.84[CEU][hapmap]
rs9818081	0.81[ASW][hapmap];0.84[CEU][hapmap];0.87[CHB][hapmap];0.97[CHD][hapmap];1.00[GIH][hapmap];0.87[JPT][hapmap];0.95[TSI][hapmap];0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9850546	0.94[AMR][1000 genomes];0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9858335	0.87[CHD][hapmap]
rs9879296	0.90[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv931072	chr3:160669567-161159779	Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	98 gene(s)	inside rSNPs	diseases
2	nsv1007004	chr3:160695108-160718154	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:160697200-160710600	Weak transcription	Left Ventricle	heart
2	chr3:160705000-160720000	Weak transcription	Gastric	stomach
3	chr3:160706000-160711200	Weak transcription	Right Atrium	heart
4	chr3:160706400-160716000	Weak transcription	Primary T cells from cord blood	blood
5	chr3:160708200-160712000	Weak transcription	Placenta	Placenta

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