Variant report

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

rs_ID	r²[population]
rs10153880	0.95[ASN][1000 genomes]
rs1025831	0.96[ASN][1000 genomes]
rs1025832	0.96[ASN][1000 genomes]
rs12470261	0.91[ASN][1000 genomes]
rs12478109	0.96[ASN][1000 genomes]
rs13393611	0.96[ASN][1000 genomes]
rs1441454	0.91[ASN][1000 genomes]
rs1837778	0.97[ASN][1000 genomes]
rs474275	0.89[AMR][1000 genomes];0.85[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs475172	0.89[AMR][1000 genomes];0.89[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs488610	0.91[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs4954843	0.91[ASN][1000 genomes]
rs4954844	0.91[ASN][1000 genomes]
rs521254	0.92[AMR][1000 genomes];0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs538308	0.89[AMR][1000 genomes];0.89[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs540441	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs540949	0.89[AMR][1000 genomes];0.89[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs567499	0.96[ASN][1000 genomes]
rs62171950	0.96[ASN][1000 genomes]
rs6747606	0.92[AMR][1000 genomes];0.88[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9646668	0.97[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv875193	chr2:141334737-141361688	Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region miRNA	n/a	inside rSNPs	n/a
2	nsv528276	chr2:141354396-141362222	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	inside rSNPs	n/a
3	nsv194547	chr2:141354994-141354996	Weak transcription	n/a	n/a	inside rSNPs	n/a

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:141351800-141359000	Weak transcription	Pancreas	Pancrea
2	chr2:141354200-141357800	Weak transcription	A549	lung

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