Variant report

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs10501590	0.81[CHB][hapmap];0.82[JPT][hapmap]
rs10792810	0.86[CHB][hapmap];0.87[JPT][hapmap]
rs10898372	0.84[ASN][1000 genomes]
rs1400630	0.81[CHB][hapmap];0.82[JPT][hapmap]
rs1517308	0.82[CHB][hapmap];0.87[JPT][hapmap]
rs1517310	0.82[CHB][hapmap];0.87[JPT][hapmap];0.88[ASN][1000 genomes]
rs1517317	0.95[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap];0.93[YRI][hapmap]
rs1914375	0.90[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap]
rs2000962	0.86[CHB][hapmap];0.82[JPT][hapmap]
rs2203702	0.86[CHB][hapmap];0.87[JPT][hapmap]
rs2449987	0.82[CHB][hapmap];0.87[JPT][hapmap];0.80[ASN][1000 genomes]
rs471786	0.81[CHB][hapmap];0.87[JPT][hapmap]
rs472630	0.82[CHB][hapmap];0.87[JPT][hapmap]
rs476791	0.86[JPT][hapmap];0.80[ASN][1000 genomes]
rs4944512	0.86[CHB][hapmap];0.87[JPT][hapmap]
rs530323	0.82[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.85[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs552017	0.87[JPT][hapmap]
rs552373	0.82[ASN][1000 genomes]
rs556710	0.86[ASN][1000 genomes]
rs580188	0.84[CHB][hapmap];0.86[JPT][hapmap]
rs601857	0.81[CHB][hapmap];0.82[JPT][hapmap]
rs7935720	0.82[CHB][hapmap];0.82[JPT][hapmap]
rs938727	0.86[CHB][hapmap];0.82[JPT][hapmap];0.83[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	nsv1044370	chr11:84748993-85293233	Enhancers Weak transcription ZNF genes & repeats Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
2	nsv1052380	chr11:84864551-84920320	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
3	nsv898042	chr11:84877221-84965437	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
4	nsv898043	chr11:84895033-85148689	Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	nsv898044	chr11:84895033-85220773	ZNF genes & repeats Flanking Bivalent TSS/Enh Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases

No data

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

No data

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