| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:56931902-56932168 | Common:3; Rare:130 | ||||
| chr16:56989463-56989574 | Common:1; Rare:20; Clinvar:1 | ||||
| chr16:57185951-57186371 | Common:1; Rare:125 | ||||
| chr16:57447360-57447503 | Common:2; Rare:40; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:58001313-58001440 | Rare:34 | ||||
| chr16:58129268-58129539 | Common:2; Rare:88 | ||||
| chr16:65121975-65122146 | Common:1; Rare:61 | ||||
| chr16:66552461-66552682 | Rare:95 | ||||
| chr16:66830896-66831052 | Rare:71 | ||||
| chr16:66934341-66934506 | Common:1; Rare:64 | ||||
| chr16:67028989-67029105 | Rare:39 | ||||
| chr16:67227011-67227196 | Rare:77 | ||||
| chr16:67481088-67481396 | Common:1; Rare:116 | ||||
| chr16:67528745-67528883 | Rare:33 | ||||
| chr16:67660227-67660366 | Rare:81; Clinvar:2; Clinvar (benign):2 |