| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:29996086-29996296 | Common:2; Rare:74 | ||||
| chr16:30065520-30065841 | Rare:113 | ||||
| chr16:30075875-30076045 | Rare:55 | ||||
| chr16:30123118-30123373 | Common:6; Rare:73 | ||||
| chr16:30183529-30183686 | Common:1; Rare:31 | ||||
| chr16:30184733-30184903 | Common:1; Rare:34 | ||||
| chr16:30355219-30355450 | Common:2; Rare:82 | ||||
| chr16:30355854-30355936 | Rare:19 | ||||
| chr16:30445871-30446055 | Common:1; Rare:45 | ||||
| chr16:30534526-30534639 | Common:1; Rare:44 | ||||
| chr16:30534761-30535079 | Common:2; Rare:98 | ||||
| chr16:30571558-30571741 | Rare:53 | ||||
| chr16:30698467-30698598 | Common:1; Rare:56 | ||||
| chr16:30748134-30748447 | Common:2; Rare:73; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:30762060-30762331 | Common:3; Rare:93 |