| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:56451303-56451567 | Common:1; Rare:73 | ||||
| chr16:56520001-56520338 | Common:6; Rare:108; Clinvar:6; Clinvar (benign):4 | ||||
| chr16:56608251-56608694 | Common:3; Rare:124 | ||||
| chr16:56625651-56625836 | Rare:52 | ||||
| chr16:56729967-56730189 | Common:1; Rare:51 | ||||
| chr16:56931915-56932155 | Common:2; Rare:116 | ||||
| chr16:57185974-57186371 | Common:1; Rare:119 | ||||
| chr16:57447360-57447502 | Common:2; Rare:40; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:58129246-58129540 | Common:2; Rare:92 | ||||
| chr16:58629772-58630022 | Common:1; Rare:71 | ||||
| chr16:62036403-62036597 | Rare:47 | ||||
| chr16:66552506-66552682 | Rare:74 | ||||
| chr16:66604415-66604674 | Rare:69 | ||||
| chr16:66934365-66934501 | Rare:48 | ||||
| chr16:67028943-67029110 | Rare:67 |