Variant report

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs10498547	0.81[ASN][1000 genomes]
rs11159470	0.91[ASN][1000 genomes]
rs11159471	0.81[ASN][1000 genomes]
rs12161870	0.82[ASN][1000 genomes]
rs12589019	0.85[ASN][1000 genomes]
rs12589109	0.91[ASN][1000 genomes]
rs17519	0.95[ASN][1000 genomes]
rs1871458	0.86[ASN][1000 genomes]
rs34201956	0.94[ASN][1000 genomes]
rs4903927	0.92[ASN][1000 genomes]
rs4903930	0.90[ASN][1000 genomes]
rs6574592	0.95[ASN][1000 genomes]
rs66523962	0.91[ASN][1000 genomes]
rs7141390	0.85[ASN][1000 genomes]
rs7142417	0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs71430713	0.81[ASN][1000 genomes]
rs7144036	0.87[ASN][1000 genomes]
rs7145447	0.81[ASN][1000 genomes]
rs7152126	0.92[ASN][1000 genomes]
rs7156452	0.85[ASN][1000 genomes]
rs7158869	0.91[ASN][1000 genomes]
rs7159302	0.91[ASN][1000 genomes]
rs8003492	0.95[ASN][1000 genomes]
rs8007955	0.84[ASN][1000 genomes]
rs8013202	0.90[ASN][1000 genomes]
rs8013610	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[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	nsv869348	chr14:80921098-81535754	Weak transcription Strong transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 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	chr14:81076200-81086600	Weak transcription	A549	lung
2	chr14:81083400-81109400	Weak transcription	Dnd41	blood
3	chr14:81083600-81088200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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