Variant report

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

rs_ID	r²[population]
rs10509696	0.90[JPT][hapmap];0.85[YRI][hapmap]
rs11188530	0.81[JPT][hapmap]
rs11819621	1.00[CHB][hapmap];0.90[JPT][hapmap]
rs11819652	1.00[CHB][hapmap];0.90[JPT][hapmap]
rs12765198	0.88[CEU][hapmap];0.85[EUR][1000 genomes]
rs12775584	0.88[CEU][hapmap];0.89[EUR][1000 genomes]
rs1414914	1.00[CHB][hapmap];0.91[JPT][hapmap];0.91[ASN][1000 genomes]
rs17111247	0.97[ASN][1000 genomes]
rs17111249	1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs2901895	1.00[CHB][hapmap];0.91[JPT][hapmap];0.97[ASN][1000 genomes]
rs3176882	1.00[CHB][hapmap]
rs3181121	1.00[CHB][hapmap]
rs34777055	0.91[EUR][1000 genomes]
rs35557930	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs57635810	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7090375	0.97[ASN][1000 genomes]
rs7093453	1.00[CHB][hapmap]
rs7100644	1.00[CHB][hapmap]
rs7904176	0.85[EUR][1000 genomes]
rs7907476	1.00[CHB][hapmap];0.90[JPT][hapmap];0.97[ASN][1000 genomes]
rs7909124	1.00[CHB][hapmap];0.90[JPT][hapmap];0.97[ASN][1000 genomes]
rs7912552	1.00[CHB][hapmap];0.90[JPT][hapmap];0.97[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2761619	chr10:97719520-97746180	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:97725400-97735800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
2	chr10:97725400-97736200	Weak transcription	GM12878-XiMat	blood

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