Variant report

Variant	rs10483756
Chromosome Location	chr14:63288002-63288003
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]
rs11158452	0.80[CHB][hapmap];0.89[JPT][hapmap]
rs12891982	0.98[AMR][1000 genomes]
rs12893269	0.94[AMR][1000 genomes]
rs12897538	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.96[GIH][hapmap];1.00[JPT][hapmap];0.81[TSI][hapmap]
rs17834917	0.90[CHB][hapmap];0.86[CHD][hapmap];1.00[JPT][hapmap]
rs2171876	1.00[JPT][hapmap];0.81[AMR][1000 genomes]
rs7493979	0.80[CHB][hapmap];0.88[JPT][hapmap];0.84[AMR][1000 genomes]
rs961066	0.85[CEU][hapmap]

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	nsv902015	chr14:63261862-63356253	Enhancers Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	n/a	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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