Variant report

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

rs_ID	r²[population]
rs10828470	0.82[AMR][1000 genomes]
rs11013531	0.91[AFR][1000 genomes];0.90[AMR][1000 genomes]
rs11013540	0.91[AFR][1000 genomes];0.91[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs11013541	0.91[AFR][1000 genomes];0.92[AMR][1000 genomes];0.81[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs11013543	0.83[AMR][1000 genomes]
rs12244668	0.81[AMR][1000 genomes]
rs12254275	0.90[AFR][1000 genomes];0.88[AMR][1000 genomes]
rs12261799	0.90[AMR][1000 genomes]
rs12263327	0.88[AFR][1000 genomes];0.88[AMR][1000 genomes]
rs12266853	0.84[AMR][1000 genomes]
rs1856113	0.81[AMR][1000 genomes]
rs1877325	0.91[AFR][1000 genomes];0.90[AMR][1000 genomes]
rs1877326	0.91[AFR][1000 genomes];0.90[AMR][1000 genomes]
rs1877327	0.91[AFR][1000 genomes];0.91[AMR][1000 genomes]
rs1877328	0.91[AFR][1000 genomes];0.91[AMR][1000 genomes]
rs1985697	0.81[AMR][1000 genomes]
rs4564227	0.84[AFR][1000 genomes];0.82[AMR][1000 genomes]
rs6482291	0.81[AMR][1000 genomes]
rs6482292	0.81[AMR][1000 genomes]
rs7904301	0.83[AFR][1000 genomes];0.86[AMR][1000 genomes]
rs7921141	0.84[AMR][1000 genomes]
rs983990	0.82[AMR][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	nsv831811	chr10:23734326-23913370	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Strong transcription Active TSS Genic enhancers ZNF genes & repeats	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:23793800-23801200	Weak transcription	K562	blood

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