Variant report

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs17047585	0.93[CHB][hapmap];0.82[JPT][hapmap];0.91[ASN][1000 genomes]
rs17047586	0.93[CHB][hapmap];0.96[CHD][hapmap];0.82[JPT][hapmap];1.00[TSI][hapmap];0.91[ASN][1000 genomes]
rs17047609	0.89[ASW][hapmap]
rs17047626	1.00[TSI][hapmap]
rs17047716	1.00[MEX][hapmap]
rs17047742	1.00[TSI][hapmap]
rs17047788	1.00[TSI][hapmap]
rs2202976	1.00[TSI][hapmap]
rs6771965	1.00[TSI][hapmap]
rs6772010	1.00[TSI][hapmap]
rs6778918	1.00[CEU][hapmap]
rs6779953	1.00[JPT][hapmap]
rs6780812	1.00[CEU][hapmap];1.00[MEX][hapmap]
rs6783583	1.00[MEX][hapmap]
rs6798891	1.00[CEU][hapmap];1.00[MEX][hapmap]
rs7433109	0.86[CHB][hapmap];0.89[CHD][hapmap];0.91[JPT][hapmap]
rs7617495	0.91[YRI][hapmap];0.91[AFR][1000 genomes]
rs7629385	1.00[CEU][hapmap];1.00[YRI][hapmap]
rs7639960	1.00[YRI][hapmap]
rs7640148	1.00[CEU][hapmap]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2752014	chr3:68091879-68416989	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
2	nsv834721	chr3:68365963-68526394	Weak transcription Enhancers ZNF genes & repeats Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
3	nsv590562	chr3:68393781-68422687	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
4	nsv590563	chr3:68402933-68422687	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases

No data

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

No data

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