Variant report

Variant	rs11693404
Chromosome Location	chr2:191007034-191007035
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 12 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs10804032	0.81[EUR][1000 genomes]
rs11687388	0.82[EUR][1000 genomes]
rs12617421	0.81[EUR][1000 genomes]
rs12990297	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs13012077	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs1357722	0.81[EUR][1000 genomes]
rs1806354	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs34377006	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs34796043	0.88[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs71434684	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7561288	0.88[AMR][1000 genomes];0.90[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	esv3439178	chr2:190877215-191124499	Enhancers Weak transcription ZNF genes & repeats Active TSS Strong transcription Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 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	chr2:190996600-191008200	Weak transcription	Aorta	Aorta

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

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