| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:67109787-67110133 | Rare:108 | ||||
| chr16:67159883-67159988 | Rare:18 | ||||
| chr16:67170453-67170549 | Common:1; Rare:14 | ||||
| chr16:67183931-67184011 | Common:1; Rare:26 | ||||
| chr16:67194401-67194624 | Rare:57 | ||||
| chr16:67227008-67227196 | Rare:80 | ||||
| chr16:67481079-67481380 | Common:1; Rare:112 | ||||
| chr16:67528745-67528890 | Rare:35 | ||||
| chr16:67537315-67537494 | Common:1; Rare:38 | ||||
| chr16:67660227-67660391 | Rare:102; Clinvar:2; Clinvar (benign):2 | ||||
| chr16:67719270-67719488 | Common:1; Rare:59 | ||||
| chr16:67806494-67806862 | Rare:83 | ||||
| chr16:67828464-67828771 | Rare:105 | ||||
| chr16:67846782-67846983 | Common:1; Rare:56 | ||||
| chr16:67935658-67935972 | Common:1; Rare:105 |