Variant report

Variant	rs73621755
Chromosome Location	chr6:130821540-130821541
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 7 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:6)

rs_ID	r²[population]
rs73620033	1.00[AFR][1000 genomes]
rs73621742	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9483131	1.00[AMR][1000 genomes]
rs9492651	1.00[AMR][1000 genomes]
rs9492664	1.00[AMR][1000 genomes]
rs9492666	1.00[AMR][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	nsv533971	chr6:130490694-131172051	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 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	chr6:130816400-130822200	Weak transcription	NHDF-Ad	bronchial
2	chr6:130816600-130821800	Weak transcription	Muscle Satellite Cultured Cells	--
3	chr6:130820400-130822200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr6:130821400-130825400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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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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