Variant report

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

rs_ID	r²[population]
rs10514723	0.84[YRI][hapmap]
rs11713541	0.86[YRI][hapmap]
rs12488594	0.94[CEU][hapmap]
rs12633931	0.94[CEU][hapmap]
rs17047774	0.92[YRI][hapmap]
rs17047798	0.94[CEU][hapmap]
rs1912458	0.90[EUR][1000 genomes]
rs2136717	0.81[EUR][1000 genomes]
rs2202976	0.87[YRI][hapmap]
rs35845454	0.84[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs4389487	0.82[EUR][1000 genomes]
rs4855474	0.85[JPT][hapmap]
rs4855475	0.86[JPT][hapmap]
rs4855480	0.83[CEU][hapmap]
rs4855483	0.94[CEU][hapmap];0.84[EUR][1000 genomes]
rs4855489	0.94[CEU][hapmap]
rs6771965	0.92[YRI][hapmap]
rs6772010	1.00[YRI][hapmap]
rs6778185	0.83[CEU][hapmap];0.83[EUR][1000 genomes]
rs6801913	0.89[CEU][hapmap];0.80[JPT][hapmap];0.92[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs6809703	0.81[YRI][hapmap]
rs73092844	0.88[EUR][1000 genomes]
rs73092847	0.88[EUR][1000 genomes]
rs73092848	0.89[EUR][1000 genomes]
rs73092849	0.89[EUR][1000 genomes]
rs907081	0.82[YRI][hapmap]
rs956352	0.83[CEU][hapmap];0.81[EUR][1000 genomes]

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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