Variant report

Variant	rs10055873
Chromosome Location	chr5:94667259-94667260
allele	C/G
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]
rs10041579	1.00[AMR][1000 genomes]
rs10057949	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10073483	1.00[AMR][1000 genomes]
rs28562390	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60872373	1.00[AMR][1000 genomes]
rs73776307	1.00[AMR][1000 genomes]
rs73777317	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	nsv432752	chr5:94524244-94691044	Flanking Bivalent TSS/Enh Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 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	chr5:94663600-94668200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr5:94667000-94667800	Enhancers	Primary monocytes fromperipheralblood	blood

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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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