| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:54286791-54287101 | Common:2; Rare:88 | ||||
| chr16:54930442-54931026 | Common:3; Rare:143 | ||||
| chr16:54931066-54931721 | Common:1; Rare:229; Clinvar:1 | ||||
| chr16:55479509-55479614 | Rare:38; Clinvar:2 | ||||
| chr16:56191000-56191600 | Common:7; Rare:200 | ||||
| chr16:56424976-56425092 | Common:1; Rare:25 | ||||
| chr16:56425440-56425830 | Common:6; Rare:135 | ||||
| chr16:56451288-56451608 | Common:1; Rare:106 | ||||
| chr16:56519418-56519818 | Common:2; Rare:210; Clinvar:5; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr16:56519977-56520219 | Common:7; Rare:91; Clinvar:6; Clinvar (benign):5 | ||||
| chr16:56608300-56608710 | Common:4; Rare:120 | ||||
| chr16:56657760-56658030 | Common:3; Rare:79 | ||||
| chr16:56682291-56682507 | Common:3; Rare:73 | ||||
| chr16:56729846-56730199 | Common:1; Rare:84 | ||||
| chr16:56931931-56932186 | Common:2; Rare:135 |