| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:66880352-66880612 | Common:2; Rare:65 | ||||
| chr16:66934327-66934528 | Common:1; Rare:83 | ||||
| chr16:67028978-67029110 | Rare:47 | ||||
| chr16:67109605-67109994 | Common:1; Rare:108 | ||||
| chr16:67159885-67159992 | Rare:18 | ||||
| chr16:67183935-67183991 | Common:1; Rare:20 | ||||
| chr16:67192103-67192240 | Common:1; Rare:51 | ||||
| chr16:67226846-67227187 | Common:1; Rare:124 | ||||
| chr16:67247447-67247738 | Rare:89 | ||||
| chr16:67481084-67481369 | Common:1; Rare:110 | ||||
| chr16:67528699-67528883 | Rare:53 | ||||
| chr16:67660222-67660375 | Rare:90; Clinvar:2; Clinvar (benign):2 | ||||
| chr16:67666711-67666853 | Rare:28 | ||||
| chr16:67719292-67719460 | Rare:44 | ||||
| chr16:67806533-67806868 | Rare:65 |