Variant report

Variant	rs72810771
Chromosome Location	chr10:22397002-22397003
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 26 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs11815737	0.87[EUR][1000 genomes]
rs12263070	0.87[EUR][1000 genomes]
rs16922008	0.87[EUR][1000 genomes]
rs16922014	0.87[EUR][1000 genomes]
rs55702118	0.87[EUR][1000 genomes]
rs55789720	0.87[EUR][1000 genomes]
rs56024469	0.87[EUR][1000 genomes]
rs56027722	1.00[EUR][1000 genomes]
rs56121502	0.87[EUR][1000 genomes]
rs56162327	1.00[EUR][1000 genomes]
rs56323200	1.00[EUR][1000 genomes]
rs66954116	0.87[EUR][1000 genomes]
rs67106981	0.87[EUR][1000 genomes]
rs72797490	0.87[EUR][1000 genomes]
rs72810732	0.87[EUR][1000 genomes]
rs72810741	0.87[EUR][1000 genomes]
rs72810756	0.87[EUR][1000 genomes]
rs72810759	0.87[EUR][1000 genomes]
rs72810761	0.87[EUR][1000 genomes]
rs72810769	0.87[EUR][1000 genomes]
rs72810772	1.00[EUR][1000 genomes]
rs72810773	1.00[EUR][1000 genomes]
rs72812739	1.00[EUR][1000 genomes]
rs72812745	0.87[EUR][1000 genomes]
rs72812756	0.87[EUR][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	nsv971872	chr10:22386395-22398112	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:22393800-22398600	Weak transcription	Fetal Stomach	stomach

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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