Variant report

Variant	rs11237072
Chromosome Location	chr11:76770641-76770642
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 10 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs11237065	0.82[EUR][1000 genomes]
rs11602496	0.83[EUR][1000 genomes]
rs11607153	0.83[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs12362167	0.83[EUR][1000 genomes]
rs12789749	0.83[EUR][1000 genomes]
rs12794060	0.83[EUR][1000 genomes]
rs7482827	0.84[AFR][1000 genomes];0.86[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs7925199	0.83[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs7949146	0.82[AFR][1000 genomes];0.86[AMR][1000 genomes];0.81[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	esv1816632	chr11:76751285-76927014	Enhancers Bivalent Enhancer Weak transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:76765000-76770800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
2	chr11:76769600-76771600	Weak transcription	Colonic Mucosa	Colon
3	chr11:76770400-76773200	Enhancers	Liver	Liver

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

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