| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:67246679-67246936 | Common:1; Rare:47 | ||||
| chr16:67247447-67247545 | Rare:37 | ||||
| chr16:67279255-67279565 | Common:1; Rare:86 | ||||
| chr16:67365219-67365323 | Rare:34 | ||||
| chr16:67393364-67393717 | Common:1; Rare:80 | ||||
| chr16:67481037-67481384 | Common:1; Rare:123 | ||||
| chr16:67528718-67528890 | Rare:46 | ||||
| chr16:67537440-67537523 | Common:2; Rare:14 | ||||
| chr16:67538226-67538754 | Common:5; Rare:187 | ||||
| chr16:67660222-67660389 | Rare:104; Clinvar:2; Clinvar (benign):2 | ||||
| chr16:67660791-67661036 | Common:2; Rare:86 | ||||
| chr16:67666715-67666870 | Rare:32 | ||||
| chr16:67719241-67719485 | Common:1; Rare:67 | ||||
| chr16:67807006-67807120 | Rare:35 | ||||
| chr16:67846482-67846983 | Common:3; Rare:146 |