Variant report

Variant	rs73085039
Chromosome Location	chr2:212601259-212601260
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 17 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs11897075	0.86[ASN][1000 genomes]
rs56005945	1.00[ASN][1000 genomes]
rs57828323	0.84[AMR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58905892	1.00[ASN][1000 genomes]
rs59605575	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62182981	1.00[ASN][1000 genomes]
rs6733874	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73069331	1.00[ASN][1000 genomes]
rs73069379	1.00[ASN][1000 genomes]
rs73085038	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73085041	1.00[EUR][1000 genomes]
rs73085065	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73085068	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7569623	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7593089	1.00[ASN][1000 genomes]
rs9784129	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][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	esv34128	chr2:212581485-212857122	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:212600800-212601800	Weak transcription	Fetal Heart	heart

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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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