| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:67028982-67029116 | Rare:45 | ||||
| chr16:67109781-67109994 | Rare:72 | ||||
| chr16:67183380-67183771 | Rare:86 | ||||
| chr16:67183923-67184052 | Common:1; Rare:38 | ||||
| chr16:67227008-67227167 | Rare:63 | ||||
| chr16:67416412-67416564 | Common:2; Rare:48 | ||||
| chr16:67481093-67481394 | Common:1; Rare:113 | ||||
| chr16:67528751-67528861 | Rare:25 | ||||
| chr16:67537370-67537494 | Common:1; Rare:24 | ||||
| chr16:67660222-67660375 | Rare:90; Clinvar:2; Clinvar (benign):2 | ||||
| chr16:67719213-67719444 | Rare:58 | ||||
| chr16:67806532-67806930 | Rare:83 | ||||
| chr16:67846718-67846976 | Common:1; Rare:69 | ||||
| chr16:67935647-67935909 | Common:1; Rare:80 | ||||
| chr16:68023209-68023302 | Common:1; Rare:25 |