Variant report

Variant	rs73919811
Chromosome Location	chr2:21295972-21295973
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs10175547	1.00[AMR][1000 genomes]
rs55867127	1.00[AMR][1000 genomes]
rs57732174	1.00[AMR][1000 genomes]
rs59056084	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59362958	1.00[AMR][1000 genomes]
rs73918050	1.00[AMR][1000 genomes]
rs73918092	1.00[AFR][1000 genomes]
rs73920524	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73921321	1.00[AMR][1000 genomes]
rs73921323	1.00[AMR][1000 genomes]
rs73921324	1.00[AMR][1000 genomes]
rs73921325	1.00[AMR][1000 genomes]
rs73921329	1.00[AMR][1000 genomes]
rs73921338	1.00[AMR][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	chr2:21295800-21296400	Enhancers	HepG2	liver

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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