Variant report

Variant	rs12703910
Chromosome Location	chr7:147151520-147151521
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 21 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs11770339	0.83[AFR][1000 genomes]
rs11771144	0.83[AFR][1000 genomes]
rs12703921	0.83[AFR][1000 genomes]
rs13222223	0.83[AFR][1000 genomes]
rs13241063	0.83[AFR][1000 genomes]
rs13242678	0.83[AFR][1000 genomes]
rs13246604	0.83[AFR][1000 genomes]
rs1358541	0.86[CEU][hapmap]
rs1406288	0.83[AFR][1000 genomes]
rs1528520	0.83[AFR][1000 genomes]
rs1842273	0.83[AFR][1000 genomes]
rs1842274	0.83[AFR][1000 genomes]
rs2373031	0.83[AFR][1000 genomes]
rs34163397	0.83[AFR][1000 genomes]
rs34959888	0.83[AFR][1000 genomes]
rs35288063	0.83[AFR][1000 genomes]
rs36103173	0.83[AFR][1000 genomes]
rs6957443	0.83[AFR][1000 genomes]
rs7457556	0.93[CEU][hapmap]
rs997223	0.83[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	nsv931005	chr7:146730472-147381257	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	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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