| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:71896176-71896236 | Common:1; Rare:19 | ||||
| chr16:72073150-72073247 | Rare:17 | ||||
| chr16:72073783-72074080 | Common:2; Rare:118 | ||||
| chr16:72074118-72074198 | Common:1; Rare:22 | ||||
| chr16:72098769-72099025 | Common:1; Rare:79 | ||||
| chr16:72099573-72099885 | Common:1; Rare:104; Clinvar (pathogenic):1 | ||||
| chr16:72107506-72107764 | Common:1; Rare:87 | ||||
| chr16:72627717-72627742 | Rare:12 | ||||
| chr16:72627764-72628047 | Common:2; Rare:77 | ||||
| chr16:72664920-72665191 | Common:1; Rare:89 | ||||
| chr16:73386500-73386833 | Common:2; Rare:58 | ||||
| chr16:73387047-73387071 | Rare:5 | ||||
| chr16:73499153-73499301 | Rare:26 | ||||
| chr16:73764009-73764185 | Rare:33 | ||||
| chr16:73811710-73811813 | Rare:26 |