Variant report

Variant	rs11984622
Chromosome Location	chr8:68433913-68433914
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 73 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:69)

rs_ID	r²[population]
rs10156292	1.00[MEX][hapmap]
rs10957389	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11989425	1.00[MEX][hapmap]
rs11990115	1.00[MEX][hapmap]
rs11994733	1.00[MEX][hapmap]
rs11994817	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11995823	1.00[MEX][hapmap]
rs11998063	1.00[MEX][hapmap]
rs12114345	1.00[MEX][hapmap]
rs12115004	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[TSI][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1393897	0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1484605	1.00[MEX][hapmap]
rs1566769	0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs16933306	1.00[MEX][hapmap]
rs16933341	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1812678	1.00[CHB][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1847292	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3824270	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4386963	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];1.00[TSI][hapmap];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs57070848	0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs57097218	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57185404	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57312956	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57714056	0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs57836294	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58637111	0.83[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs59607772	0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs60606572	0.83[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs61142861	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61220075	0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs61679446	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6472300	1.00[CHD][hapmap];1.00[JPT][hapmap];1.00[TSI][hapmap]
rs6472301	1.00[CHD][hapmap];1.00[JPT][hapmap];1.00[TSI][hapmap]
rs6472303	1.00[JPT][hapmap]
rs6472306	1.00[JPT][hapmap]
rs6472307	1.00[CHD][hapmap];1.00[JPT][hapmap];1.00[TSI][hapmap]
rs6472308	1.00[JPT][hapmap]
rs6472314	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[TSI][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6651314	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7005010	1.00[CHD][hapmap];1.00[JPT][hapmap];1.00[TSI][hapmap]
rs7009065	1.00[CHD][hapmap];1.00[JPT][hapmap];1.00[TSI][hapmap]
rs7013505	1.00[MEX][hapmap]
rs7018199	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[TSI][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73262665	0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs73262669	0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs73262675	0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs73262680	0.94[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs73262681	0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs73262685	0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs73262686	0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs73262688	0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs73262691	0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs73262695	0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs73262696	0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs73264707	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73264769	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73264774	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73264780	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73264784	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73264792	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73264794	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7341614	1.00[CEU][hapmap]
rs7815213	0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7824691	1.00[JPT][hapmap]
rs7839073	1.00[JPT][hapmap]
rs7842960	1.00[JPT][hapmap]
rs7843818	1.00[JPT][hapmap]
rs966593	1.00[CEU][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs966594	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2752263	chr8:68170946-68788493	Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
2	nsv1024135	chr8:68235792-68629789	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
3	nsv539642	chr8:68235792-68629789	Weak transcription Flanking Bivalent TSS/Enh Enhancers Strong transcription Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
4	esv2752264	chr8:68244546-68647201	Enhancers Flanking Active TSS Weak transcription Strong transcription Bivalent Enhancer ZNF genes & repeats Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:68424800-68434200	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr8:68424800-68435000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr8:68433400-68434800	Enhancers	HMEC	breast
4	chr8:68433600-68434000	Enhancers	NHEK	skin
5	chr8:68433800-68435400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin

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