Variant report

Variant	rs7943164
Chromosome Location	chr11:26411934-26411935
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 86 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:85)

rs_ID	r²[population]
rs10047414	0.85[CHB][hapmap]
rs10047464	0.85[CHB][hapmap]
rs1037899	0.81[CHB][hapmap]
rs1037900	0.81[CHB][hapmap]
rs10742138	0.83[CHB][hapmap]
rs10742139	0.85[CHB][hapmap]
rs10767520	0.87[ASN][1000 genomes]
rs10767526	0.85[CHB][hapmap]
rs10767527	0.85[CHB][hapmap]
rs10767531	0.84[CHB][hapmap]
rs10767535	0.85[CHB][hapmap]
rs10834974	0.84[CHB][hapmap]
rs11029538	0.81[AFR][1000 genomes];0.84[AMR][1000 genomes]
rs11029543	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11029552	0.84[CHB][hapmap]
rs11500182	0.84[CHB][hapmap]
rs11824236	0.82[CHB][hapmap];0.86[JPT][hapmap];0.94[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12098873	0.90[CHB][hapmap];0.89[JPT][hapmap];0.94[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12270746	0.89[CHB][hapmap];0.88[JPT][hapmap]
rs12274334	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12274387	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12275964	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12283791	1.00[CHB][hapmap];0.88[JPT][hapmap]
rs12287530	0.81[CHB][hapmap];0.85[JPT][hapmap];0.97[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12287626	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12288668	0.83[CHB][hapmap]
rs12294597	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12294604	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13377552	0.93[CHB][hapmap]
rs1381174	0.85[CHB][hapmap]
rs1381177	0.90[CHB][hapmap];0.89[JPT][hapmap];0.95[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1381181	0.84[ASN][1000 genomes]
rs1381183	0.84[ASN][1000 genomes]
rs1461364	0.90[CHB][hapmap];0.89[JPT][hapmap]
rs1461365	0.90[CHB][hapmap];0.88[JPT][hapmap]
rs1461366	0.90[CHB][hapmap];0.88[JPT][hapmap]
rs1461368	0.81[CHB][hapmap]
rs1461373	0.90[CHB][hapmap];0.88[JPT][hapmap]
rs1461374	0.94[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1461376	0.92[ASN][1000 genomes]
rs1461377	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1461380	1.00[CHB][hapmap];0.88[JPT][hapmap]
rs1461382	0.95[CHB][hapmap];0.82[JPT][hapmap]
rs1461384	1.00[CHB][hapmap]
rs1461385	1.00[CHB][hapmap];0.83[JPT][hapmap]
rs1563958	0.85[CHB][hapmap]
rs16915597	1.00[CHB][hapmap];0.88[JPT][hapmap]
rs1993745	0.90[CHB][hapmap]
rs2006942	1.00[CHB][hapmap];0.88[JPT][hapmap];1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2045703	0.81[CHB][hapmap]
rs2085878	0.94[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2085879	0.94[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2085880	0.90[CHB][hapmap];0.88[JPT][hapmap];0.94[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2126184	0.86[ASN][1000 genomes]
rs2126185	0.92[ASN][1000 genomes]
rs2199376	0.94[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2350206	0.85[CHB][hapmap]
rs4032918	0.85[CHB][hapmap]
rs4923354	0.81[CHB][hapmap];0.86[ASN][1000 genomes]
rs61877724	0.94[AFR][1000 genomes];0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs67498125	0.81[EUR][1000 genomes]
rs7102859	0.84[CHB][hapmap]
rs7104759	0.92[CHB][hapmap]
rs7107402	0.85[CHB][hapmap]
rs7113405	0.84[CHB][hapmap]
rs7123118	0.84[CHB][hapmap]
rs7123997	0.81[CHB][hapmap]
rs7124839	0.90[CHB][hapmap];0.88[JPT][hapmap]
rs7128615	0.86[ASN][1000 genomes]
rs716701	0.86[ASN][1000 genomes]
rs719106	0.90[CHB][hapmap];0.88[JPT][hapmap]
rs7480892	1.00[CHB][hapmap];0.88[JPT][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7925120	0.88[CHB][hapmap]
rs7925575	0.85[CHB][hapmap]
rs7925675	0.86[CHB][hapmap];0.82[JPT][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7928015	0.90[CHB][hapmap];0.89[JPT][hapmap]
rs7931439	1.00[CHB][hapmap];0.88[JPT][hapmap]
rs7936431	0.85[CHB][hapmap]
rs7940514	1.00[CHB][hapmap];0.88[JPT][hapmap]
rs7942291	0.90[CHB][hapmap];0.88[JPT][hapmap]
rs7945645	0.94[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7946083	0.90[CHB][hapmap];0.89[JPT][hapmap];0.94[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs961685	1.00[CHB][hapmap];0.89[JPT][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9943473	1.00[CHB][hapmap];0.83[JPT][hapmap]
rs9943594	1.00[CHB][hapmap];0.88[JPT][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	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

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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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