Variant report

Variant	rs17050031
Chromosome Location	chr2:59488019-59488020
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 9 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs11125778	0.85[CHB][hapmap];0.94[JPT][hapmap];0.82[ASN][1000 genomes]
rs13017760	0.85[ASN][1000 genomes]
rs1558596	0.86[EUR][1000 genomes]
rs62148582	0.82[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs6713914	0.83[EUR][1000 genomes]
rs6727119	0.85[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs7586283	0.97[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs7588177	0.85[EUR][1000 genomes];0.81[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	nsv834170	chr2:59436676-59604794	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:59484000-59493600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
2	chr2:59487800-59488800	Weak transcription	HUES48 Cell Line	embryonic stem cell
3	chr2:59487800-59493000	Weak transcription	iPS-15b Cell Line	embryonic stem cell

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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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