Variant report

Variant	rs7073982
Chromosome Location	chr10:26494512-26494513
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 20 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs10508715	0.91[JPT][hapmap];0.83[ASN][1000 genomes]
rs11014995	0.82[ASN][1000 genomes]
rs11014996	0.81[CHB][hapmap];0.91[JPT][hapmap];0.85[ASN][1000 genomes]
rs1330572	0.91[JPT][hapmap]
rs1330581	0.83[CEU][hapmap];0.81[JPT][hapmap]
rs2236417	0.83[ASN][1000 genomes]
rs2236418	0.91[JPT][hapmap];0.83[ASN][1000 genomes]
rs2839669	0.83[ASN][1000 genomes]
rs2839670	0.91[JPT][hapmap];0.83[ASN][1000 genomes]
rs2839671	0.91[JPT][hapmap];0.83[ASN][1000 genomes]
rs3758446	0.83[ASN][1000 genomes]
rs3847378	0.86[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs61839365	0.81[ASN][1000 genomes]
rs7071922	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7072136	0.83[ASN][1000 genomes]
rs8190582	0.83[ASN][1000 genomes]
rs8190598	0.83[ASN][1000 genomes]
rs8190647	0.83[JPT][hapmap]
rs994502	0.91[JPT][hapmap];0.83[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	nsv894975	chr10:26343356-27014467	Strong transcription Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	25 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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