Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:67562166-67562623 | Common:1; Rare:144 | ||||
chr16:67562735-67563179 | Common:3; Rare:128 | ||||
chr16:67644767-67644953 | Rare:44 | ||||
chr16:67645039-67645263 | Common:1; Rare:59 | ||||
chr16:67660147-67660473 | Rare:175; Clinvar:3; Clinvar (benign):2 | ||||
chr16:67660690-67661088 | Common:3; Rare:135 | ||||
chr16:67666689-67666868 | Rare:37 | ||||
chr16:67667339-67667448 | Common:1; Rare:24 | ||||
chr16:67685822-67685979 | Rare:17 | ||||
chr16:67719268-67719709 | Common:1; Rare:105 | ||||
chr16:67806476-67806939 | Rare:111 | ||||
chr16:67806965-67807108 | Rare:42 | ||||
chr16:67833771-67834032 | Common:1; Rare:99 | ||||
chr16:67841866-67842441 | Common:2; Rare:167 | ||||
chr16:67842694-67842838 | Rare:31; Clinvar (pathogenic):1 |