Variant report

Variant	rs11158471
Chromosome Location	chr14:63528514-63528515
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 31 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:28)

rs_ID	r²[population]
rs10132722	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10134176	0.95[CEU][hapmap];0.83[MEX][hapmap];0.94[TSI][hapmap]
rs10136314	0.95[CEU][hapmap]
rs10147103	0.95[CEU][hapmap];0.83[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs10162413	0.83[ASN][1000 genomes]
rs10873166	1.00[CEU][hapmap];0.82[CHB][hapmap]
rs1111450	0.87[MEX][hapmap]
rs1950983	0.87[MEX][hapmap]
rs1950985	0.95[CEU][hapmap];0.91[CHB][hapmap];0.87[JPT][hapmap]
rs1956670	1.00[ASW][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.93[LWK][hapmap];0.87[MEX][hapmap];1.00[YRI][hapmap]
rs2146940	0.87[MEX][hapmap]
rs2356101	0.94[CEU][hapmap];0.82[CHB][hapmap]
rs3850312	0.83[ASW][hapmap];0.95[CEU][hapmap];0.82[CHB][hapmap];0.89[CHD][hapmap];0.88[GIH][hapmap];0.83[MEX][hapmap];0.94[TSI][hapmap]
rs3915801	0.83[ASW][hapmap];0.82[CHB][hapmap];0.89[CHD][hapmap];0.87[MEX][hapmap]
rs4127778	0.95[CEU][hapmap];0.81[CHB][hapmap]
rs4127780	0.83[ASW][hapmap];0.95[CEU][hapmap];0.82[CHB][hapmap];0.89[CHD][hapmap];0.88[GIH][hapmap];0.83[MEX][hapmap];0.94[TSI][hapmap];0.89[AMR][1000 genomes];0.88[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4483779	0.87[MEX][hapmap]
rs4584750	0.82[CHB][hapmap]
rs6573480	0.95[CEU][hapmap];0.83[MEX][hapmap];0.94[TSI][hapmap];0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs7141839	0.83[ASW][hapmap];0.95[CEU][hapmap];0.88[GIH][hapmap];0.92[TSI][hapmap];0.87[EUR][1000 genomes]
rs7159344	0.95[CEU][hapmap];0.84[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs8006668	0.95[CEU][hapmap]
rs8015817	0.82[CHB][hapmap]
rs8017368	0.86[CHB][hapmap]
rs8018618	0.91[ASN][1000 genomes]
rs8019140	0.87[MEX][hapmap]
rs8020935	0.95[CEU][hapmap];0.82[CHB][hapmap]
rs941709	0.83[ASW][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.95[JPT][hapmap];0.87[MEX][hapmap];0.97[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv527251	chr14:63400786-64068806	Flanking Bivalent TSS/Enh Weak transcription Strong transcription Flanking Active TSS Enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
2	nsv520528	chr14:63400786-64157117	Weak transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
3	nsv564893	chr14:63526931-63796122	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	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
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