Variant report

Variant	rs10767519
Chromosome Location	chr11:26402783-26402784
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 44 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:43)

rs_ID	r²[population]
rs1037899	0.96[CEU][hapmap];0.93[CHB][hapmap];0.86[JPT][hapmap]
rs1037900	0.96[CEU][hapmap];0.94[CHB][hapmap];0.86[JPT][hapmap]
rs10767520	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11029543	0.86[ASN][1000 genomes]
rs11824236	0.91[ASN][1000 genomes]
rs12098873	0.80[CHB][hapmap];0.91[ASN][1000 genomes]
rs12274334	0.85[ASN][1000 genomes]
rs12274387	0.85[ASN][1000 genomes]
rs12275964	0.87[ASN][1000 genomes]
rs12287530	0.82[JPT][hapmap];0.86[ASN][1000 genomes]
rs12287626	0.85[ASN][1000 genomes]
rs12294597	0.86[ASN][1000 genomes]
rs12294604	0.87[ASN][1000 genomes]
rs13377552	0.85[CHB][hapmap]
rs1381177	0.80[CHB][hapmap];0.91[ASN][1000 genomes]
rs1381181	0.96[CEU][hapmap];0.87[CHB][hapmap];0.86[JPT][hapmap];0.91[AFR][1000 genomes];0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1381183	0.96[CEU][hapmap];0.86[CHB][hapmap];0.85[JPT][hapmap];0.94[AFR][1000 genomes];0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1461364	0.80[CHB][hapmap]
rs1461368	0.93[CHB][hapmap];0.86[JPT][hapmap]
rs1461374	0.91[ASN][1000 genomes]
rs1461376	0.91[AMR][1000 genomes];0.84[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1461377	0.87[ASN][1000 genomes]
rs1993745	0.96[CEU][hapmap];0.87[CHB][hapmap]
rs2006942	0.87[ASN][1000 genomes]
rs2045703	0.96[CEU][hapmap];0.94[CHB][hapmap];0.86[JPT][hapmap]
rs2085878	0.89[ASN][1000 genomes]
rs2085879	0.91[ASN][1000 genomes]
rs2085880	0.91[ASN][1000 genomes]
rs2126184	0.95[AFR][1000 genomes];0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2126185	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2199376	0.91[ASN][1000 genomes]
rs4923354	0.96[CEU][hapmap];0.93[CHB][hapmap];0.86[JPT][hapmap];0.94[AFR][1000 genomes];0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs61877724	0.90[ASN][1000 genomes]
rs7104759	0.86[CHB][hapmap]
rs7123997	0.96[CEU][hapmap];0.93[CHB][hapmap];0.86[JPT][hapmap]
rs7128615	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs716701	0.91[CEU][hapmap];0.92[CHB][hapmap];0.98[AFR][1000 genomes];0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7480892	0.87[ASN][1000 genomes]
rs7925675	0.86[CHB][hapmap];0.81[JPT][hapmap];0.91[ASN][1000 genomes]
rs7928015	0.80[CHB][hapmap]
rs7945645	0.91[ASN][1000 genomes]
rs7946083	0.80[CHB][hapmap];0.91[ASN][1000 genomes]
rs961685	0.87[ASN][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	esv2422406	chr11:26329870-26473641	Flanking Bivalent TSS/Enh Enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Weak transcription ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

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

No data

Quick Search:

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

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links