| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:46689130-46689416 | Common:1; Rare:102; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:46973627-46973781 | Rare:70 | ||||
| chr16:47461027-47461362 | Common:2; Rare:125; Clinvar (benign):2 | ||||
| chr16:53703814-53704194 | Rare:113; Clinvar:4; Clinvar (benign):1 | ||||
| chr16:54286397-54286465 | Rare:13 | ||||
| chr16:54286688-54287016 | Common:2; Rare:94 | ||||
| chr16:55479037-55479207 | Rare:41 | ||||
| chr16:56451306-56451563 | Common:1; Rare:70 | ||||
| chr16:56682091-56682494 | Common:7; Rare:104 | ||||
| chr16:56729949-56730198 | Common:1; Rare:60 | ||||
| chr16:56989382-56989607 | Common:1; Rare:53; Clinvar:1 | ||||
| chr16:57185981-57186342 | Common:1; Rare:104 | ||||
| chr16:57244982-57245256 | Common:3; Rare:89 | ||||
| chr16:57447360-57447507 | Common:2; Rare:40; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:58115531-58115740 | Rare:33 |