| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:70346804-70346994 | Common:2; Rare:94 | ||||
| chr16:70454568-70454638 | Rare:20 | ||||
| chr16:70523478-70523872 | Common:3; Rare:147; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr16:70679988-70680147 | Rare:50 | ||||
| chr16:71230625-71230861 | Common:1; Rare:78; Clinvar (benign):1 | ||||
| chr16:71289341-71289459 | Rare:37 | ||||
| chr16:71358630-71358763 | Rare:50 | ||||
| chr16:71462150-71462273 | Common:2; Rare:57 | ||||
| chr16:71489290-71489385 | Common:1; Rare:34 | ||||
| chr16:71564911-71565029 | Common:1; Rare:41 | ||||
| chr16:71723770-71724052 | Common:5; Rare:98 | ||||
| chr16:71808320-71808452 | Rare:49 | ||||
| chr16:71808461-71808505 | Rare:15 | ||||
| chr16:71808766-71809009 | Common:1; Rare:106 | ||||
| chr16:71809034-71809360 | Common:3; Rare:104 |