Variant report

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs10462022	0.99[ASN][1000 genomes]
rs12517050	1.00[ASN][1000 genomes]
rs12518582	0.84[AFR][1000 genomes];0.83[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs12655176	1.00[ASN][1000 genomes]
rs16871412	1.00[ASN][1000 genomes]
rs16871449	0.99[ASN][1000 genomes]
rs17207595	1.00[ASN][1000 genomes]
rs2859816	0.99[ASN][1000 genomes]
rs318017	0.83[AMR][1000 genomes]
rs318020	0.86[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs318021	0.84[AMR][1000 genomes]
rs3851440	0.99[ASN][1000 genomes]
rs3851441	0.99[ASN][1000 genomes]
rs3851442	0.99[ASN][1000 genomes]
rs3913717	0.97[ASN][1000 genomes]
rs3913718	0.97[ASN][1000 genomes]
rs3913719	0.97[ASN][1000 genomes]
rs3913720	0.97[ASN][1000 genomes]
rs4559040	1.00[ASN][1000 genomes]
rs4957156	0.83[AMR][1000 genomes]
rs4957158	0.82[AMR][1000 genomes]
rs508669	0.83[AMR][1000 genomes]
rs55803511	0.93[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs56182059	0.92[ASN][1000 genomes]
rs57159430	0.99[ASN][1000 genomes]
rs58203282	1.00[ASN][1000 genomes]
rs59751170	0.99[ASN][1000 genomes]
rs627744	0.82[AMR][1000 genomes]
rs6870727	0.99[ASN][1000 genomes]
rs694218	0.82[AMR][1000 genomes]
rs7703079	0.96[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	esv3386611	chr5:41494995-41498593	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:41494400-41504600	Weak transcription	Ovary	ovary
2	chr5:41495800-41507000	Weak transcription	Left Ventricle	heart
3	chr5:41497200-41498400	Enhancers	Pancreatic Islets	Pancreatic Islet
4	chr5:41497800-41504000	Enhancers	Fetal Heart	heart

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