Variant report

Variant	rs6484203
Chromosome Location	chr11:26357771-26357772
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 4 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:3)

rs_ID	r²[population]
rs11029484	0.86[CEU][hapmap]
rs11029522	0.92[CEU][hapmap]
rs72876916	0.88[AMR][1000 genomes];0.88[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	esv2422406	chr11:26329870-26473641	Flanking Bivalent TSS/Enh Enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Weak transcription ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:26354000-26361400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr11:26355600-26358000	Enhancers	HUES64 Cell Line	embryonic stem cell
3	chr11:26356800-26358000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr11:26357200-26357800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr11:26357200-26357800	Enhancers	NHDF-Ad	bronchial
6	chr11:26357200-26357800	Enhancers	Osteobl	bone
7	chr11:26357200-26358000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr11:26357200-26358000	Enhancers	Fetal Stomach	stomach
9	chr11:26357400-26357800	Enhancers	Fetal Lung	lung
10	chr11:26357600-26357800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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