Variant report

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs12488594	0.83[JPT][hapmap]
rs12633931	0.83[CHB][hapmap];0.93[GIH][hapmap];0.94[TSI][hapmap]
rs13076798	0.83[MKK][hapmap]
rs17047647	0.83[MKK][hapmap]
rs17047650	0.83[MKK][hapmap]
rs17047798	0.83[JPT][hapmap]
rs1912458	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2136716	0.86[MKK][hapmap]
rs2175517	0.91[ASN][1000 genomes]
rs35845454	0.91[EUR][1000 genomes]
rs4277695	0.83[MKK][hapmap]
rs4855482	0.85[GIH][hapmap];0.88[TSI][hapmap]
rs4855483	0.87[CHB][hapmap];0.83[EUR][1000 genomes]
rs4855489	0.84[CHD][hapmap];0.93[GIH][hapmap];0.90[JPT][hapmap];0.87[MKK][hapmap];0.94[TSI][hapmap]
rs6766759	0.86[JPT][hapmap]
rs6778185	0.82[CHB][hapmap];0.87[CHD][hapmap];0.93[GIH][hapmap];0.91[TSI][hapmap]
rs6801913	0.86[GIH][hapmap];0.88[TSI][hapmap];0.89[EUR][1000 genomes]
rs73092844	0.83[EUR][1000 genomes]
rs73092847	0.83[EUR][1000 genomes]
rs73092848	0.84[EUR][1000 genomes]
rs73092849	0.84[EUR][1000 genomes]
rs7634101	1.00[LWK][hapmap];0.95[MKK][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	esv1832396	chr3:68478762-68641509	Enhancers Weak transcription ZNF genes & repeats Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
2	nsv876929	chr3:68508137-68565824	ZNF genes & repeats Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No data

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