| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:30650735-30651021 | Rare:88 | ||||
| chr16:30658593-30658864 | Common:1; Rare:82 | ||||
| chr16:30660101-30660187 | Rare:17 | ||||
| chr16:30697905-30698240 | Common:1; Rare:144 | ||||
| chr16:30698459-30698644 | Common:1; Rare:72 | ||||
| chr16:30699035-30699394 | Rare:87; Clinvar (benign):1 | ||||
| chr16:30762056-30762343 | Common:3; Rare:93 | ||||
| chr16:30893932-30894275 | Common:5; Rare:93 | ||||
| chr16:30896437-30896624 | Common:1; Rare:45 | ||||
| chr16:30923251-30923612 | Common:1; Rare:86 | ||||
| chr16:31033233-31033627 | Common:2; Rare:117 | ||||
| chr16:31073673-31073848 | Rare:55 | ||||
| chr16:31074187-31074483 | Common:1; Rare:84 | ||||
| chr16:31201779-31202121 | Rare:140 | ||||
| chr16:31202591-31202805 | Rare:80 |