| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:53054960-53055055 | Rare:16 | ||||
| chr16:53703809-53704187 | Rare:113; Clinvar:4; Clinvar (benign):1 | ||||
| chr16:54286741-54287020 | Common:1; Rare:87 | ||||
| chr16:56451289-56451605 | Common:1; Rare:103 | ||||
| chr16:56608276-56608756 | Common:4; Rare:134 | ||||
| chr16:56625589-56625812 | Common:1; Rare:67 | ||||
| chr16:56682304-56682488 | Common:3; Rare:58 | ||||
| chr16:56729988-56730198 | Common:1; Rare:48 | ||||
| chr16:56931939-56932173 | Common:2; Rare:122 | ||||
| chr16:56936579-56936802 | Rare:58 | ||||
| chr16:56989505-56989605 | Common:1; Rare:25 | ||||
| chr16:57185784-57186461 | Common:4; Rare:190 | ||||
| chr16:57244964-57245285 | Common:3; Rare:104 | ||||
| chr16:57447350-57447514 | Common:2; Rare:45; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:57619843-57620116 | Rare:55 |