Variant report

Variant	rs7993335
Chromosome Location	chr13:97707152-97707153
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 22 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs10162251	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs10467249	0.85[EUR][1000 genomes]
rs1501858	0.83[AFR][1000 genomes]
rs1604445	0.85[EUR][1000 genomes]
rs16953709	0.85[EUR][1000 genomes]
rs60668201	0.85[EUR][1000 genomes]
rs60711187	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs7323760	0.85[EUR][1000 genomes]
rs7333674	0.85[EUR][1000 genomes]
rs7982736	0.82[AFR][1000 genomes]
rs7983750	0.82[AFR][1000 genomes]
rs7993469	0.87[AFR][1000 genomes]
rs8001111	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs9582094	0.85[EUR][1000 genomes]
rs9582103	0.83[AFR][1000 genomes]
rs9584459	0.85[EUR][1000 genomes]
rs9584462	0.85[EUR][1000 genomes]
rs9584464	0.85[EUR][1000 genomes]
rs9584465	0.85[EUR][1000 genomes]
rs9584470	0.82[AFR][1000 genomes]
rs992706	0.81[AFR][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	nsv832693	chr13:97594845-97777481	Bivalent/Poised TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	8 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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