Variant report

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs11919968	0.94[YRI][hapmap];1.00[AMR][1000 genomes]
rs11921652	0.94[YRI][hapmap]
rs13320595	1.00[AMR][1000 genomes]
rs13325188	0.83[YRI][hapmap];1.00[AMR][1000 genomes]
rs13353520	1.00[AMR][1000 genomes]
rs17023810	0.94[YRI][hapmap];1.00[AMR][1000 genomes]
rs17024695	0.82[YRI][hapmap]
rs1900791	0.94[YRI][hapmap]
rs28611113	1.00[AMR][1000 genomes]
rs4473548	0.94[YRI][hapmap];0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57661808	1.00[AMR][1000 genomes]
rs6549066	0.85[YRI][hapmap];0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6762825	1.00[AMR][1000 genomes]
rs6764756	1.00[AMR][1000 genomes]
rs6796380	0.81[YRI][hapmap]
rs72910511	1.00[AMR][1000 genomes]
rs72910559	1.00[AMR][1000 genomes]
rs72912429	1.00[AMR][1000 genomes]
rs72912437	1.00[AMR][1000 genomes]
rs72912471	1.00[AMR][1000 genomes]
rs72912474	1.00[AMR][1000 genomes]
rs7622132	0.82[YRI][hapmap]
rs7636187	0.84[YRI][hapmap]
rs7649694	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7650035	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9811856	0.93[YRI][hapmap]
rs9816884	0.94[YRI][hapmap]
rs9840424	0.89[YRI][hapmap]
rs9856802	1.00[AMR][1000 genomes]
rs9863493	0.82[YRI][hapmap]
rs9872154	1.00[AMR][1000 genomes]
rs9874223	1.00[AMR][1000 genomes]
rs9876097	1.00[AMR][1000 genomes]
rs9880094	1.00[AMR][1000 genomes]

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	nsv532629	chr3:85763873-86608579	Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases

No data

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

No data

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