| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:66933918-66934711 | Common:2; Rare:246 | ||||
| chr16:66935340-66935699 | Common:1; Rare:138 | ||||
| chr16:67028959-67029143 | Rare:63 | ||||
| chr16:67109834-67110014 | Rare:60 | ||||
| chr16:67159884-67160009 | Rare:20 | ||||
| chr16:67170420-67170551 | Common:1; Rare:21 | ||||
| chr16:67183560-67183780 | Rare:58 | ||||
| chr16:67183931-67184028 | Common:1; Rare:30 | ||||
| chr16:67199098-67199163 | Common:1; Rare:25 | ||||
| chr16:67227008-67227201 | Rare:83 | ||||
| chr16:67393479-67393663 | Common:1; Rare:42 | ||||
| chr16:67481057-67481380 | Common:1; Rare:116 | ||||
| chr16:67528568-67528883 | Rare:75 | ||||
| chr16:67660222-67660373 | Rare:89; Clinvar:2; Clinvar (benign):2 | ||||
| chr16:67660761-67661052 | Common:2; Rare:101 |