Variant report

Variant	rs1470834
Chromosome Location	chr8:78069284-78069285
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs10086637	0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10095652	0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11990859	0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11992889	0.85[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs16939427	0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs16939431	0.91[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs16939459	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs16939460	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs16939462	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs1840079	0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4644212	0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7004978	0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs716468	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes];0.80[ASN][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	nsv891045	chr8:77998659-78477561	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 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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