| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:67805044-67805675 | Common:1; Rare:157 | ||||
| chr16:67860950-67861400 | Common:1; Rare:80 | ||||
| chr16:67947999-67948410 | Rare:232 | ||||
| chr16:68377570-68378040 | Common:3; Rare:84 | ||||
| chr16:68406798-68407082 | Common:1; Rare:59 | ||||
| chr16:68416400-68416770 | Common:1; Rare:81 | ||||
| chr16:68417706-68418250 | Common:1; Rare:137 | ||||
| chr16:68434830-68435210 | Common:2; Rare:59 | ||||
| chr16:68658570-68659130 | Common:7; Rare:193 | ||||
| chr16:68669280-68669610 | Common:2; Rare:50 | ||||
| chr16:68707570-68708106 | Common:4; Rare:229 | ||||
| chr16:68722495-68722615 | Common:2; Rare:14 | ||||
| chr16:68731920-68732220 | Common:3; Rare:58 | ||||
| chr16:68732818-68733026 | Common:2; Rare:33 | ||||
| chr16:68737879-68738595 | Common:1; Rare:175; Clinvar:19; Clinvar (benign):26 |