Variant report

Variant	rs11824171
Chromosome Location	chr11:45616902-45616903
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]
rs11820172	1.00[EUR][1000 genomes]
rs11821506	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11825398	0.85[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs11826256	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12276259	1.00[EUR][1000 genomes]
rs45480804	1.00[EUR][1000 genomes]
rs45535741	1.00[EUR][1000 genomes]
rs73456092	1.00[EUR][1000 genomes]
rs895730	1.00[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	nsv897310	chr11:45487041-45631953	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:45615000-45626200	Weak transcription	Fetal Brain Male	brain
2	chr11:45616200-45617400	Enhancers	Fetal Lung	lung
3	chr11:45616400-45617400	Enhancers	Fetal Stomach	stomach
4	chr11:45616600-45617400	Enhancers	Brain Germinal Matrix	brain

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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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