Variant report

rSNPs within LD-proxies of this variant (count:28)

rs_ID	r²[population]
rs11937701	0.83[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs11939049	0.83[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs12502649	0.83[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs12511624	0.80[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs12512723	0.88[AFR][1000 genomes];0.88[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs12512727	0.88[AFR][1000 genomes];0.85[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs13136231	0.96[YRI][hapmap]
rs4293757	1.00[CHB][hapmap]
rs58441575	0.83[AFR][1000 genomes];0.95[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs59407249	0.83[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs61792875	0.84[ASN][1000 genomes]
rs61792876	0.84[ASN][1000 genomes]
rs61792877	0.84[ASN][1000 genomes]
rs61792878	0.84[ASN][1000 genomes]
rs61792882	0.84[ASN][1000 genomes]
rs61792933	0.84[ASN][1000 genomes]
rs61792936	0.84[ASN][1000 genomes]
rs6448729	0.84[ASN][1000 genomes]
rs6846615	1.00[CHB][hapmap];0.84[ASN][1000 genomes]
rs6847898	0.84[ASN][1000 genomes]
rs73113461	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73113466	0.98[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73113470	0.97[AFR][1000 genomes];0.95[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs73113475	0.83[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs73113481	0.83[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs73113482	0.83[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs7676542	1.00[CHB][hapmap];0.84[ASN][1000 genomes]
rs9985629	0.84[ASN][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	nsv998450	chr4:30823631-31628179	Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
2	nsv878811	chr4:30987395-31019279	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:30998000-31018000	Weak transcription	Aorta	Aorta
2	chr4:31007200-31012600	Weak transcription	Fetal Heart	heart
3	chr4:31009400-31022000	Weak transcription	Fetal Stomach	stomach

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