Variant report

Variant	rs72920735
Chromosome Location	chr6:71669239-71669240
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 17 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs10945278	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs11757574	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs12524190	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs12529422	0.93[EUR][1000 genomes]
rs2347632	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs2347633	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs4479893	0.82[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs4506005	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs55870610	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs56291137	0.82[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs6927786	0.91[EUR][1000 genomes]
rs7451863	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs7746949	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs7774025	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs9283838	0.90[EUR][1000 genomes]
rs9294883	0.82[AMR][1000 genomes];0.93[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	nsv886148	chr6:71623253-71694742	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Weak transcription	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:0 , 50 per page) page:

No data

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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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