Variant report

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs17047606	0.89[CHB][hapmap];0.86[JPT][hapmap]
rs17047609	0.89[CHB][hapmap];0.86[JPT][hapmap]
rs17047611	0.89[CHB][hapmap];0.93[JPT][hapmap]
rs2221759	0.95[CHB][hapmap];1.00[JPT][hapmap];0.95[MEX][hapmap]
rs262186	0.89[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.89[YRI][hapmap]
rs262190	0.88[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap]
rs262193	0.88[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap]
rs262200	0.95[CHB][hapmap];1.00[JPT][hapmap];0.81[AMR][1000 genomes]
rs262201	0.82[AMR][1000 genomes]
rs262202	0.89[CEU][hapmap];0.95[CHB][hapmap];0.93[JPT][hapmap];0.86[MEX][hapmap]
rs262204	0.89[CEU][hapmap];0.89[CHB][hapmap];0.93[JPT][hapmap];0.95[MEX][hapmap];0.84[AMR][1000 genomes]
rs262206	0.85[CEU][hapmap];0.89[CHB][hapmap];0.86[JPT][hapmap];0.91[MEX][hapmap]
rs262226	0.91[MEX][hapmap]
rs262227	0.91[MEX][hapmap]
rs262234	0.84[CHB][hapmap]
rs262238	0.86[MEX][hapmap]
rs262241	0.86[MEX][hapmap]
rs63108	0.86[MEX][hapmap]
rs6769848	0.85[CHB][hapmap];0.87[JPT][hapmap]
rs6776111	0.90[CHB][hapmap];0.87[JPT][hapmap]
rs7610318	0.95[CHB][hapmap];1.00[JPT][hapmap];0.95[MEX][hapmap]
rs7629299	0.90[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap]
rs7629408	0.90[CHB][hapmap];0.87[JPT][hapmap]
rs952768	0.95[CHB][hapmap];1.00[JPT][hapmap];0.95[MEX][hapmap]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv834721	chr3:68365963-68526394	Weak transcription Enhancers ZNF genes & repeats Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
2	nsv998582	chr3:68422687-68461190	Enhancers ZNF genes & repeats Active TSS 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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