Variant report

rSNPs within LD-proxies of this variant (count:39)

rs_ID	r²[population]
rs10188432	1.00[CHB][hapmap]
rs11891221	1.00[CHB][hapmap]
rs11897270	1.00[CHB][hapmap]
rs12990666	1.00[CHB][hapmap]
rs12999683	1.00[CHB][hapmap]
rs13003828	1.00[CHB][hapmap]
rs13007837	1.00[CHB][hapmap]
rs13030114	1.00[CHB][hapmap]
rs1401117	1.00[CHB][hapmap]
rs1518443	1.00[CHB][hapmap]
rs1518444	1.00[CHB][hapmap]
rs1518445	1.00[CHB][hapmap]
rs1518446	1.00[CHB][hapmap]
rs16843964	1.00[CHB][hapmap]
rs16843975	1.00[CHB][hapmap]
rs16843984	1.00[CHB][hapmap]
rs16843999	1.00[CHB][hapmap]
rs16844001	1.00[CHB][hapmap]
rs17387299	1.00[CHB][hapmap]
rs1878741	1.00[CHB][hapmap]
rs1878742	1.00[CHB][hapmap]
rs1949452	1.00[CHB][hapmap]
rs2030240	1.00[CHB][hapmap]
rs2030241	1.00[CHB][hapmap]
rs4293513	1.00[CHB][hapmap]
rs474837	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs487419	1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[YRI][hapmap]
rs491391	1.00[CHB][hapmap];0.89[YRI][hapmap];0.92[AFR][1000 genomes];0.94[EUR][1000 genomes]
rs492190	1.00[CHB][hapmap];0.89[YRI][hapmap];0.92[AFR][1000 genomes];0.94[EUR][1000 genomes]
rs494227	0.92[AFR][1000 genomes];0.94[EUR][1000 genomes]
rs503742	0.82[CEU][hapmap];1.00[CHB][hapmap];0.95[YRI][hapmap];0.95[AFR][1000 genomes];0.97[EUR][1000 genomes]
rs524037	1.00[EUR][1000 genomes]
rs538467	0.93[AFR][1000 genomes];0.93[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs540307	0.92[AFR][1000 genomes];0.94[EUR][1000 genomes]
rs6723181	1.00[CHB][hapmap]
rs6730266	1.00[CHB][hapmap]
rs6744731	1.00[CHB][hapmap]
rs6747180	1.00[CHB][hapmap]
rs7581949	1.00[CHB][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	nsv583193	chr2:141365171-141415043	Active TSS Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	n/a

No data

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

No data

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