Variant report

Variant	rs7610597
Chromosome Location	chr3:22435368-22435369
allele	G/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]
rs11129055	0.80[CHB][hapmap];0.80[JPT][hapmap]
rs11129060	0.84[CEU][hapmap];0.94[CHB][hapmap]
rs11129061	0.85[CHB][hapmap]
rs12492984	0.92[CEU][hapmap];1.00[CHB][hapmap];0.95[CHD][hapmap];1.00[GIH][hapmap];0.90[JPT][hapmap];0.91[TSI][hapmap]
rs13061996	0.85[CHB][hapmap];0.90[CHD][hapmap];0.85[JPT][hapmap]
rs1494228	0.91[CEU][hapmap];1.00[CHB][hapmap];0.84[JPT][hapmap]
rs1494230	0.84[CEU][hapmap];1.00[CHB][hapmap];0.92[CHD][hapmap];1.00[GIH][hapmap];0.90[JPT][hapmap];0.91[TSI][hapmap]
rs1548136	0.84[CEU][hapmap];1.00[CHB][hapmap];0.92[CHD][hapmap];1.00[GIH][hapmap];0.85[JPT][hapmap];0.85[TSI][hapmap]
rs2047156	0.83[CHB][hapmap];0.87[CHD][hapmap];0.80[JPT][hapmap]
rs2047159	0.83[CHB][hapmap];0.85[JPT][hapmap]
rs2198020	0.84[CEU][hapmap];0.94[CHB][hapmap];0.82[CHD][hapmap];0.90[JPT][hapmap];0.88[TSI][hapmap]
rs4431131	0.83[ASW][hapmap];0.92[LWK][hapmap];0.96[MKK][hapmap];0.85[TSI][hapmap];0.96[YRI][hapmap]
rs4858035	0.84[CEU][hapmap];0.85[JPT][hapmap]
rs6768103	0.83[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6789629	0.82[CHD][hapmap];0.84[JPT][hapmap]
rs7642830	0.85[CEU][hapmap];1.00[CHB][hapmap];0.90[JPT][hapmap];0.96[YRI][hapmap]
rs7645719	0.84[CEU][hapmap];1.00[CHB][hapmap];0.85[JPT][hapmap]
rs935737	0.85[CEU][hapmap];1.00[CHB][hapmap];0.90[JPT][hapmap]
rs9798951	0.85[CEU][hapmap];0.88[CHB][hapmap];0.89[JPT][hapmap];0.92[YRI][hapmap]
rs982354	0.84[CEU][hapmap];1.00[CHB][hapmap];0.90[CHD][hapmap];1.00[GIH][hapmap];0.90[JPT][hapmap];0.88[TSI][hapmap];0.83[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs986483	0.84[CEU][hapmap];1.00[CHB][hapmap];0.90[CHD][hapmap];1.00[GIH][hapmap];0.90[JPT][hapmap];0.85[TSI][hapmap]
rs9882784	0.84[CEU][hapmap];1.00[CHB][hapmap];0.84[JPT][hapmap];0.95[EUR][1000 genomes];0.91[ASN][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	nsv1003211	chr3:22244883-22584229	Weak transcription Bivalent/Poised TSS Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv536520	chr3:22244883-22584229	Enhancers Bivalent/Poised TSS Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv428082	chr3:22397625-22539817	Weak transcription Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv834634	chr3:22420053-22574021	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	nsv526662	chr3:22426918-22441261	Enhancers Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:0 , 50 per page) page:

No data

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dbSNP/dbVar ID: rs12345 /nsv7879
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