Variant report

Variant	rs17526489
Chromosome Location	chr13:88452338-88452339
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs2027158	1.00[CHB][hapmap];0.88[JPT][hapmap];0.85[ASN][1000 genomes]
rs2027159	0.97[ASN][1000 genomes]
rs2152246	0.91[ASN][1000 genomes]
rs2152247	0.95[ASN][1000 genomes]
rs7997375	0.84[ASN][1000 genomes]
rs9513930	1.00[CHB][hapmap];0.88[JPT][hapmap];0.97[ASN][1000 genomes]
rs9513950	0.95[ASN][1000 genomes]
rs9513962	0.89[ASN][1000 genomes]
rs9518492	1.00[CHB][hapmap];0.93[ASN][1000 genomes]
rs9518507	0.97[ASN][1000 genomes]
rs9518509	0.93[ASN][1000 genomes]
rs9518545	0.82[ASN][1000 genomes]
rs9645867	0.84[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv562631	chr13:88379124-88470185	Active TSS Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv832673	chr13:88431110-88607319	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:0 , 50 per page) page:

No data

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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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