Variant report

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs10509697	0.88[CEU][hapmap];0.89[EUR][1000 genomes]
rs11596697	1.00[CHD][hapmap]
rs11599105	0.87[CEU][hapmap];0.82[YRI][hapmap];0.84[EUR][1000 genomes]
rs12761082	0.84[EUR][1000 genomes]
rs12762284	0.86[CEU][hapmap];0.82[AFR][1000 genomes];0.86[EUR][1000 genomes]
rs12765198	1.00[CEU][hapmap];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs12769120	0.87[CEU][hapmap]
rs3181115	1.00[CHD][hapmap]
rs34777055	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs35298116	0.84[EUR][1000 genomes]
rs35557930	0.91[EUR][1000 genomes]
rs35864527	0.84[EUR][1000 genomes]
rs4918979	0.86[ASW][hapmap];1.00[LWK][hapmap];0.95[YRI][hapmap]
rs57635810	0.87[EUR][1000 genomes]
rs66530311	0.84[EUR][1000 genomes]
rs66851219	0.93[AFR][1000 genomes];0.88[EUR][1000 genomes]
rs67166869	0.84[EUR][1000 genomes]
rs67870248	0.93[AFR][1000 genomes];0.88[EUR][1000 genomes]
rs7904176	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs7922216	0.87[TSI][hapmap]

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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