| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:69762251-69762385 | Common:1; Rare:35 | ||||
| chr16:69950397-69950735 | Common:3; Rare:25 | ||||
| chr16:69951077-69951295 | Rare:17 | ||||
| chr16:70173154-70173320 | Common:1; Rare:17 | ||||
| chr16:70173412-70173794 | Common:1; Rare:49 | ||||
| chr16:70299117-70299252 | Rare:27 | ||||
| chr16:70346751-70346952 | Common:1; Rare:99 | ||||
| chr16:70523513-70523872 | Common:3; Rare:123; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr16:71564917-71564996 | Common:1; Rare:30 | ||||
| chr16:71723821-71724062 | Common:5; Rare:86 | ||||
| chr16:71808754-71808826 | Rare:45 | ||||
| chr16:71808828-71808869 | Common:1; Rare:14 | ||||
| chr16:71809048-71809348 | Common:3; Rare:99 | ||||
| chr16:71845920-71846029 | Common:1; Rare:35 | ||||
| chr16:71895404-71895574 | Rare:55 |