Variant report

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs1020686	0.92[ASN][1000 genomes]
rs1037595	0.91[ASN][1000 genomes]
rs1037596	0.92[ASN][1000 genomes]
rs1124176	0.95[CHB][hapmap];0.95[JPT][hapmap]
rs1334172	0.92[ASN][1000 genomes]
rs1455406	0.92[ASN][1000 genomes]
rs1760825	0.92[ASN][1000 genomes]
rs1760826	0.92[ASN][1000 genomes]
rs3963390	0.84[MEX][hapmap]
rs4415893	0.86[CHB][hapmap];0.95[JPT][hapmap];0.94[ASN][1000 genomes]
rs4432131	0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.90[AFR][1000 genomes];0.97[AMR][1000 genomes];0.91[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4771593	0.92[ASN][1000 genomes]
rs7332979	0.90[ASN][1000 genomes]
rs7987813	0.95[CHB][hapmap];0.95[JPT][hapmap]
rs8002849	0.95[CHB][hapmap];0.95[CHD][hapmap];0.95[JPT][hapmap]
rs9514921	0.85[ASN][1000 genomes]
rs9514980	0.95[CHB][hapmap];0.95[CHD][hapmap];0.95[JPT][hapmap];0.84[MEX][hapmap];0.97[ASN][1000 genomes]
rs9521103	0.91[ASN][1000 genomes]
rs9521138	0.95[CHB][hapmap];0.95[JPT][hapmap]
rs9559491	0.84[MEX][hapmap]
rs9587692	0.86[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	nsv900815	chr13:89098616-89216190	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv870345	chr13:89164439-89295782	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

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

No data

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