| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:56931896-56932163 | Common:3; Rare:127 | ||||
| chr16:56989384-56989585 | Common:1; Rare:47; Clinvar:1 | ||||
| chr16:57185987-57186371 | Common:1; Rare:118 | ||||
| chr16:57447371-57447502 | Common:2; Rare:36; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:58129274-58129567 | Common:3; Rare:94 | ||||
| chr16:58629810-58630133 | Common:2; Rare:87 | ||||
| chr16:65121959-65122355 | Common:1; Rare:122 | ||||
| chr16:65124277-65124424 | Rare:24 | ||||
| chr16:66751587-66751917 | Common:3; Rare:93 | ||||
| chr16:66934366-66934506 | Rare:50 | ||||
| chr16:67159899-67159994 | Rare:17 | ||||
| chr16:67227008-67227160 | Rare:60 | ||||
| chr16:67481090-67481373 | Common:1; Rare:107 | ||||
| chr16:67528701-67528847 | Rare:43 | ||||
| chr16:67660263-67660373 | Rare:62; Clinvar:2; Clinvar (benign):1 |