Variant report

Variant	rs56220205
Chromosome Location	chr3:150574202-150574203
allele	G/T
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]
rs16862868	1.00[EUR][1000 genomes]
rs16862916	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs57454586	1.00[EUR][1000 genomes]
rs58991236	1.00[EUR][1000 genomes]
rs6777167	0.97[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73871604	1.00[EUR][1000 genomes]
rs73871606	1.00[EUR][1000 genomes]
rs73871609	1.00[EUR][1000 genomes]
rs73871613	0.91[AFR][1000 genomes];0.87[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	nsv532662	chr3:150180747-150633414	Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	101 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	chr3:150574000-150574400	Enhancers	Primary neutrophils fromperipheralblood	blood
2	chr3:150574200-150575200	Enhancers	Placenta	Placenta

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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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