| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:56931934-56932187 | Common:2; Rare:136 | ||||
| chr16:56989360-56989605 | Common:1; Rare:56; Clinvar:1 | ||||
| chr16:57185683-57185906 | Common:3; Rare:52 | ||||
| chr16:57185951-57186442 | Common:2; Rare:144 | ||||
| chr16:57244976-57245376 | Common:3; Rare:132 | ||||
| chr16:57284626-57284766 | Common:2; Rare:44 | ||||
| chr16:57447354-57447536 | Common:2; Rare:55; Clinvar:2; Clinvar (benign):3 | ||||
| chr16:57619676-57619782 | Common:1; Rare:27 | ||||
| chr16:57619961-57620127 | Rare:37 | ||||
| chr16:57628501-57628703 | Common:3; Rare:49 | ||||
| chr16:57668150-57668325 | Common:1; Rare:35 | ||||
| chr16:57774839-57775057 | Common:2; Rare:33 | ||||
| chr16:57999491-57999622 | Rare:25 | ||||
| chr16:58001318-58001633 | Common:1; Rare:112; Clinvar (benign):1 | ||||
| chr16:58025646-58025764 | Rare:41 |