Variant report

Variant	rs62355271
Chromosome Location	chr5:35846145-35846146
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 39 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:38)

rs_ID	r²[population]
rs10472982	0.82[EUR][1000 genomes]
rs10491434	0.91[EUR][1000 genomes]
rs10491435	0.91[EUR][1000 genomes]
rs1053496	0.91[EUR][1000 genomes]
rs11567685	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs11567699	0.81[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs11567701	0.81[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs11567751	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs11949736	0.84[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11950763	0.83[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11952663	0.86[ASN][1000 genomes]
rs11958811	0.83[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11960511	0.89[EUR][1000 genomes]
rs1494554	0.80[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1494571	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1603071	0.84[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2361395	0.83[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs3194051	0.92[EUR][1000 genomes]
rs35968532	0.94[ASN][1000 genomes]
rs3822733	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs4263525	0.80[EUR][1000 genomes]
rs56113663	0.82[EUR][1000 genomes]
rs56123112	0.84[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs56133736	0.81[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57217480	0.84[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs57545288	0.81[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs57804084	0.83[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs62351973	0.84[EUR][1000 genomes]
rs62353742	0.84[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs62355269	0.84[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62355272	0.84[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs67207043	0.87[EUR][1000 genomes]
rs700179	0.91[EUR][1000 genomes]
rs7718034	0.83[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7725599	0.82[EUR][1000 genomes]
rs7733008	0.84[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9292614	0.82[EUR][1000 genomes]
rs987107	0.92[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	nsv1022761	chr5:35775802-35902546	Enhancers Weak transcription Genic enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 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	chr5:35843000-35847000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr5:35844600-35846600	ZNF genes & repeats	Dnd41	blood
3	chr5:35845400-35846200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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