Variant report

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs1022184	0.87[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs13434171	0.81[CEU][hapmap]
rs1397249	0.87[CEU][hapmap];0.89[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs1397250	0.87[CEU][hapmap];0.89[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs1397251	1.00[CEU][hapmap]
rs1510362	1.00[CEU][hapmap]
rs1510365	0.87[CEU][hapmap]
rs17047774	0.82[YRI][hapmap]
rs1858242	0.89[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs2137178	0.88[CEU][hapmap]
rs2175266	0.90[JPT][hapmap]
rs2175518	0.88[CEU][hapmap]
rs2202976	0.81[YRI][hapmap]
rs2202978	0.87[CEU][hapmap];0.90[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2665529	0.87[CEU][hapmap];0.90[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs2665534	0.86[CEU][hapmap];0.87[AMR][1000 genomes]
rs2665544	0.87[CEU][hapmap];0.89[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs4488833	0.88[CEU][hapmap];0.90[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs4855488	0.86[YRI][hapmap]
rs6764527	0.83[AMR][1000 genomes]
rs6765886	0.81[CEU][hapmap]
rs6771965	0.85[YRI][hapmap]
rs6772010	0.93[YRI][hapmap]
rs6801032	0.88[CEU][hapmap]
rs9867056	1.00[CEU][hapmap]

Variant overlapped rSNPs/rCNVs (count:1 , 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

No data

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

No data

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