Variant report

Variant	rs11760118
Chromosome Location	chr6:150718738-150718739
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 8 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs12203809	0.88[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs13197942	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs34257671	1.00[ASN][1000 genomes]
rs73000920	1.00[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs73000923	1.00[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs9478733	1.00[ASN][1000 genomes]
rs9480385	1.00[AFR][1000 genomes];1.00[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	esv2763602	chr6:150581193-150720666	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:150712200-150719200	Weak transcription	Fetal Intestine Small	intestine
2	chr6:150718200-150721800	Strong transcription	Liver	Liver

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

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