Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:21376708..21379043-chr2:21381243..21383355,2	K562	blood:

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

rs_ID	r²[population]
rs1003177	1.00[EUR][1000 genomes]
rs11886946	0.82[ASN][1000 genomes]
rs11892905	0.88[ASN][1000 genomes]
rs11893753	0.99[ASN][1000 genomes]
rs11899839	0.85[ASN][1000 genomes]
rs11900335	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12172886	0.89[ASN][1000 genomes]
rs13306194	1.00[EUR][1000 genomes]
rs1544977	0.85[ASN][1000 genomes]
rs17041973	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2059972	1.00[EUR][1000 genomes]
rs2337384	0.88[ASN][1000 genomes]
rs57666320	0.85[ASN][1000 genomes]
rs57825321	1.00[EUR][1000 genomes]
rs60132502	1.00[ASN][1000 genomes]
rs60403956	0.99[ASN][1000 genomes]
rs61086479	0.89[ASN][1000 genomes]
rs61142046	0.92[ASN][1000 genomes]
rs61407223	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6757883	0.88[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	nsv873728	chr2:21250914-21460786	Enhancers Bivalent Enhancer Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:21372200-21377000	Weak transcription	HepG2	liver

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