Variant report

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs10155009	1.00[CHB][hapmap];0.81[CHD][hapmap];0.85[GIH][hapmap];1.00[JPT][hapmap]
rs13319937	1.00[YRI][hapmap]
rs13434171	1.00[YRI][hapmap]
rs1397251	0.86[CHB][hapmap];1.00[YRI][hapmap]
rs1397253	0.82[ASW][hapmap];0.81[CEU][hapmap];1.00[YRI][hapmap]
rs1491743	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1491756	1.00[CHB][hapmap];0.85[GIH][hapmap];1.00[JPT][hapmap]
rs1491757	1.00[CHB][hapmap];0.85[GIH][hapmap];1.00[JPT][hapmap]
rs169023	1.00[CHB][hapmap];1.00[CHD][hapmap];0.91[GIH][hapmap];1.00[JPT][hapmap];0.91[MEX][hapmap];1.00[MKK][hapmap];1.00[YRI][hapmap]
rs1858372	1.00[YRI][hapmap]
rs1858373	1.00[YRI][hapmap]
rs187794	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs2175518	1.00[YRI][hapmap]
rs262217	1.00[YRI][hapmap]
rs4345072	1.00[CHB][hapmap];0.81[CHD][hapmap];0.85[GIH][hapmap]
rs4378971	1.00[CHB][hapmap]
rs4488833	1.00[YRI][hapmap]
rs6549116	1.00[CHB][hapmap];0.89[CHD][hapmap];0.82[GIH][hapmap];1.00[JPT][hapmap];0.86[MEX][hapmap];0.82[ASN][1000 genomes]
rs6770136	1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[ASN][1000 genomes]
rs6782797	0.82[ASW][hapmap];1.00[YRI][hapmap]
rs6783358	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs6804831	1.00[YRI][hapmap]
rs7614996	1.00[CHB][hapmap];0.90[CHD][hapmap];0.88[GIH][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs7623705	1.00[YRI][hapmap]
rs7634667	1.00[YRI][hapmap]
rs9310118	1.00[YRI][hapmap]
rs9867056	0.82[ASW][hapmap];1.00[YRI][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

Quick Search:

Input of quick search could be: