| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:67806511-67806926 | Rare:95 | ||||
| chr16:67842247-67842561 | Common:1; Rare:99 | ||||
| chr16:67846811-67847238 | Common:2; Rare:117 | ||||
| chr16:67935647-67935972 | Common:1; Rare:111 | ||||
| chr16:67936786-67937143 | Common:2; Rare:64 | ||||
| chr16:67942726-67943007 | Common:1; Rare:83; Clinvar (pathogenic):4 | ||||
| chr16:67945860-67946014 | Rare:50 | ||||
| chr16:67968497-67968863 | Common:2; Rare:127 | ||||
| chr16:67998822-67999050 | Common:1; Rare:43 | ||||
| chr16:68000518-68000760 | Rare:45 | ||||
| chr16:68023207-68023302 | Common:1; Rare:26 | ||||
| chr16:68234751-68234837 | Rare:15 | ||||
| chr16:68245151-68245468 | Common:1; Rare:95 | ||||
| chr16:68264408-68264688 | Rare:81 | ||||
| chr16:68265284-68265475 | Rare:28 |