Variant report

Variant	rs1064250
Chromosome Location	chr6:70926334-70926335
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 27 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs1200575	0.92[CEU][hapmap];0.95[GIH][hapmap];0.89[TSI][hapmap];0.94[EUR][1000 genomes]
rs1201814	1.00[CHB][hapmap];0.97[CHD][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12204439	0.84[EUR][1000 genomes]
rs1517042	0.92[CEU][hapmap];0.87[GIH][hapmap];0.89[TSI][hapmap];0.94[EUR][1000 genomes]
rs1736	0.92[CEU][hapmap];0.95[GIH][hapmap];0.89[TSI][hapmap];0.94[EUR][1000 genomes]
rs2176355	0.92[CEU][hapmap];0.94[EUR][1000 genomes]
rs2296005	0.96[CEU][hapmap];0.93[EUR][1000 genomes]
rs2296010	0.88[CEU][hapmap];0.87[TSI][hapmap];0.87[EUR][1000 genomes]
rs34147000	0.87[EUR][1000 genomes]
rs3793059	0.81[EUR][1000 genomes]
rs4544872	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6908735	0.92[CEU][hapmap];0.84[GIH][hapmap];0.84[TSI][hapmap];0.87[EUR][1000 genomes]
rs6909913	0.91[CEU][hapmap];0.88[EUR][1000 genomes]
rs6920170	0.92[CEU][hapmap];0.87[GIH][hapmap];0.89[TSI][hapmap];0.94[EUR][1000 genomes]
rs6928201	0.81[EUR][1000 genomes]
rs6933155	0.94[EUR][1000 genomes]
rs9360412	0.94[EUR][1000 genomes]
rs9360413	0.94[EUR][1000 genomes]
rs9360414	0.92[CEU][hapmap];0.84[GIH][hapmap];0.89[TSI][hapmap];0.94[EUR][1000 genomes]
rs9360416	0.88[CEU][hapmap];0.91[EUR][1000 genomes]
rs9364075	0.81[EUR][1000 genomes]
rs9364077	0.87[CEU][hapmap];0.88[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1026151	chr6:70621616-70946967	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv933674	chr6:70663616-70973112	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Active TSS Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv932111	chr6:70736835-71633094	Enhancers Active TSS Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
4	nsv886142	chr6:70741209-71251421	Weak transcription Strong transcription Enhancers Bivalent/Poised TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
5	nsv830683	chr6:70743422-70941190	Bivalent Enhancer Enhancers Weak transcription Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:70918600-70930800	Weak transcription	Primary B cells from peripheral blood	blood

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