Variant report

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

rs_ID	r²[population]
rs10843773	0.95[ASN][1000 genomes]
rs2086899	1.00[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs4931347	0.81[ASN][1000 genomes]
rs57800469	1.00[EUR][1000 genomes]
rs57865433	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58828862	1.00[ASN][1000 genomes]
rs58849181	1.00[EUR][1000 genomes]
rs59540862	1.00[EUR][1000 genomes]
rs59849223	1.00[EUR][1000 genomes]
rs59971700	1.00[EUR][1000 genomes]
rs60094407	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61330126	1.00[EUR][1000 genomes]
rs61921137	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73083724	1.00[ASN][1000 genomes]
rs73083730	1.00[ASN][1000 genomes]
rs73287313	1.00[EUR][1000 genomes]
rs73287348	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs74082420	1.00[EUR][1000 genomes]
rs74084145	1.00[EUR][1000 genomes]
rs7968211	0.95[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	esv3343291	chr12:30455597-30992837	Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	48 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:30672600-30681200	Weak transcription	K562	blood
2	chr12:30672600-30686800	Weak transcription	Ovary	ovary
3	chr12:30678400-30680000	Weak transcription	Pancreas	Pancrea

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