| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:29925345-29925785 | Common:1; Rare:157 | ||||
| chr16:29926031-29926406 | Common:9; Rare:318 | ||||
| chr16:29961657-29962227 | Common:3; Rare:307 | ||||
| chr16:29962775-29962985 | Common:2; Rare:39 | ||||
| chr16:29973440-29974009 | Common:12; Rare:340 | ||||
| chr16:29995580-29995792 | Common:3; Rare:241 | ||||
| chr16:29995850-29996555 | Common:9; Rare:545 | ||||
| chr16:30010840-30011470 | Common:4; Rare:350 | ||||
| chr16:30021253-30021498 | Rare:102 | ||||
| chr16:30021534-30021860 | Rare:80 | ||||
| chr16:30052893-30053343 | Common:3; Rare:297; Clinvar (benign):3 | ||||
| chr16:30053740-30054682 | Common:3; Rare:178 | ||||
| chr16:30064901-30065384 | Rare:264 | ||||
| chr16:30065326-30065938 | Rare:522 | ||||
| chr16:30066080-30067830 | Common:6; Rare:796; Clinvar:8; Clinvar (benign):4 |