Variant report

Variant	rs62133263
Chromosome Location	chr2:21374231-21374232
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 26 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs11693760	0.85[AFR][1000 genomes];0.87[EUR][1000 genomes]
rs11693775	0.85[AFR][1000 genomes];0.89[EUR][1000 genomes]
rs11693870	0.86[EUR][1000 genomes]
rs12052779	0.88[EUR][1000 genomes]
rs17395333	0.90[AFR][1000 genomes];0.91[EUR][1000 genomes]
rs17395512	1.00[AFR][1000 genomes];0.94[EUR][1000 genomes]
rs17399144	0.82[AFR][1000 genomes];0.89[EUR][1000 genomes]
rs1897083	0.85[EUR][1000 genomes]
rs2115838	0.85[AFR][1000 genomes];0.96[EUR][1000 genomes]
rs2163203	0.83[AFR][1000 genomes];0.93[EUR][1000 genomes]
rs2195597	0.85[AFR][1000 genomes];0.93[EUR][1000 genomes]
rs2337383	0.96[AFR][1000 genomes];0.91[EUR][1000 genomes]
rs2878956	0.93[AFR][1000 genomes];0.95[EUR][1000 genomes]
rs4665176	0.85[AFR][1000 genomes];0.89[EUR][1000 genomes]
rs4665178	0.86[EUR][1000 genomes]
rs4665179	0.86[EUR][1000 genomes]
rs56079819	0.85[EUR][1000 genomes]
rs56090741	0.96[AFR][1000 genomes];0.89[EUR][1000 genomes]
rs56201838	0.85[AFR][1000 genomes];0.91[EUR][1000 genomes]
rs56306424	0.85[AFR][1000 genomes];0.92[EUR][1000 genomes]
rs61539677	0.85[EUR][1000 genomes]
rs62122520	0.84[EUR][1000 genomes]
rs62133264	0.93[AFR][1000 genomes];0.96[EUR][1000 genomes]
rs62135035	1.00[AFR][1000 genomes];0.94[EUR][1000 genomes]
rs754523	0.85[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	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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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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