| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:53703798-53704215 | Common:1; Rare:132; Clinvar:5; Clinvar (benign):2 | ||||
| chr16:54286731-54286968 | Common:1; Rare:69 | ||||
| chr16:56191215-56191503 | Common:1; Rare:97 | ||||
| chr16:56451092-56451615 | Common:3; Rare:174 | ||||
| chr16:56608466-56608704 | Common:2; Rare:75 | ||||
| chr16:56625727-56625849 | Rare:39 | ||||
| chr16:56657589-56658086 | Common:4; Rare:135 | ||||
| chr16:56729945-56730235 | Common:1; Rare:70 | ||||
| chr16:56931942-56932181 | Common:2; Rare:126 | ||||
| chr16:57092589-57092619 | Rare:10 | ||||
| chr16:57185736-57186455 | Common:4; Rare:199 | ||||
| chr16:57244970-57245358 | Common:3; Rare:131 | ||||
| chr16:57284626-57284771 | Common:2; Rare:46 | ||||
| chr16:57372408-57372511 | Rare:19 | ||||
| chr16:57447342-57447549 | Common:2; Rare:70; Clinvar:2; Clinvar (benign):4 |