Variant report

Variant	rs880732
Chromosome Location	chr14:83266017-83266018
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 22 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs10484138	0.86[ASN][1000 genomes]
rs11627025	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs12587660	0.86[ASN][1000 genomes]
rs12590200	0.84[ASN][1000 genomes]
rs17117384	0.86[ASN][1000 genomes]
rs17117392	0.86[ASN][1000 genomes]
rs28654536	0.83[EUR][1000 genomes]
rs35768970	0.86[ASN][1000 genomes]
rs7150950	0.86[ASN][1000 genomes]
rs73355432	0.80[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs74067200	0.86[ASN][1000 genomes]
rs74067202	0.86[ASN][1000 genomes]
rs74069203	0.86[ASN][1000 genomes]
rs74069241	0.86[ASN][1000 genomes]
rs74069243	0.86[ASN][1000 genomes]
rs74069244	0.86[ASN][1000 genomes]
rs74069245	0.82[ASN][1000 genomes]
rs74069248	0.86[ASN][1000 genomes]
rs74069249	0.86[ASN][1000 genomes]
rs74069251	0.86[ASN][1000 genomes]
rs9323726	0.83[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	nsv902124	chr14:83165520-83282163	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	1 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	chr14:83265600-83266400	Enhancers	Aorta	Aorta

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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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