Variant report

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

rs_ID	r²[population]
rs11992507	1.00[EUR][1000 genomes]
rs11996308	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16926906	1.00[EUR][1000 genomes]
rs16926938	1.00[EUR][1000 genomes]
rs1835758	1.00[EUR][1000 genomes]
rs56031720	1.00[EUR][1000 genomes]
rs59775198	1.00[EUR][1000 genomes]
rs60420622	1.00[EUR][1000 genomes]
rs73685726	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73685727	1.00[EUR][1000 genomes]
rs73685728	1.00[EUR][1000 genomes]
rs73685729	0.98[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73685730	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73685732	1.00[EUR][1000 genomes]
rs73685733	1.00[EUR][1000 genomes]
rs73685734	1.00[EUR][1000 genomes]
rs73685735	1.00[EUR][1000 genomes]
rs73685738	0.81[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73685740	1.00[EUR][1000 genomes]
rs73685742	1.00[EUR][1000 genomes]
rs73685743	1.00[EUR][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	nsv948922	chr8:61818964-62475097	Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 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	chr8:62025400-62027800	Enhancers	GM12878-XiMat	blood

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