| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:58001289-58001540 | Common:1; Rare:87; Clinvar (benign):1 | ||||
| chr16:58025650-58025815 | Rare:70 | ||||
| chr16:58128747-58128884 | Common:1; Rare:28 | ||||
| chr16:58129254-58129800 | Common:8; Rare:182 | ||||
| chr16:58198070-58198390 | Common:3; Rare:103 | ||||
| chr16:58249852-58250084 | Rare:66 | ||||
| chr16:58392278-58392501 | Common:3; Rare:59 | ||||
| chr16:58392787-58392898 | Common:2; Rare:27 | ||||
| chr16:58464789-58465599 | Common:3; Rare:230 | ||||
| chr16:58495121-58495450 | Common:2; Rare:63 | ||||
| chr16:58495579-58495775 | Common:3; Rare:57 | ||||
| chr16:58499887-58500145 | Common:2; Rare:41 | ||||
| chr16:58501340-58501590 | Common:1; Rare:61 | ||||
| chr16:58515408-58515538 | Common:2; Rare:51 | ||||
| chr16:58629764-58630222 | Common:3; Rare:128 |