Variant report

Variant	rs2511534
Chromosome Location	chr8:113867117-113867118
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 43 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:38)

rs_ID	r²[population]
rs10081489	0.86[JPT][hapmap]
rs10106945	0.89[ASN][1000 genomes]
rs10216505	0.89[ASN][1000 genomes]
rs12334432	0.89[JPT][hapmap];0.89[ASN][1000 genomes]
rs13261060	0.89[JPT][hapmap]
rs1549354	0.89[JPT][hapmap]
rs1991136	0.91[GIH][hapmap];0.89[JPT][hapmap];0.89[ASN][1000 genomes]
rs1991137	0.86[GIH][hapmap];0.89[JPT][hapmap];0.89[ASN][1000 genomes]
rs2113666	0.86[GIH][hapmap];0.89[JPT][hapmap];0.87[ASN][1000 genomes]
rs2161925	0.89[JPT][hapmap]
rs231279	0.89[JPT][hapmap];0.87[ASN][1000 genomes]
rs231281	0.89[JPT][hapmap];0.89[ASN][1000 genomes]
rs231286	0.89[JPT][hapmap];0.89[ASN][1000 genomes]
rs2355821	0.89[JPT][hapmap]
rs2432736	0.84[MEX][hapmap]
rs2432737	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs2432738	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs2432739	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[TSI][hapmap]
rs2432742	0.86[GIH][hapmap];0.89[JPT][hapmap];0.89[ASN][1000 genomes]
rs2446470	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2446471	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2446472	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs2511531	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs2511532	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs4876480	0.89[JPT][hapmap]
rs61584754	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6999481	0.86[GIH][hapmap];0.89[JPT][hapmap];0.89[ASN][1000 genomes]
rs7004983	0.88[JPT][hapmap]
rs7005129	0.89[JPT][hapmap]
rs72680285	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7817596	0.89[ASN][1000 genomes]
rs7817723	0.89[JPT][hapmap]
rs7817836	0.89[JPT][hapmap];0.89[ASN][1000 genomes]
rs7832050	0.89[JPT][hapmap]
rs889987	0.89[JPT][hapmap]
rs9297478	0.88[JPT][hapmap]
rs9297479	0.89[JPT][hapmap]
rs9297480	0.86[GIH][hapmap];0.89[JPT][hapmap];0.89[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2753595	chr8:113283214-114190390	Enhancers Weak transcription Active TSS Strong transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	6 gene(s)	inside rSNPs	diseases
2	nsv534270	chr8:113585830-113979075	Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA	3 gene(s)	inside rSNPs	diseases
3	esv2754315	chr8:113736824-114048824	ZNF genes & repeats Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	nsv891326	chr8:113777669-114091732	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	nsv891327	chr8:113828980-114109342	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh	Chromatin interactive region	1 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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