| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:47461038-47461398 | Common:3; Rare:138; Clinvar (benign):3 | ||||
| chr16:48244253-48244430 | Common:2; Rare:60 | ||||
| chr16:53703814-53704187 | Rare:109; Clinvar:4; Clinvar (benign):1 | ||||
| chr16:56451296-56451567 | Common:1; Rare:75 | ||||
| chr16:56608440-56608694 | Common:2; Rare:78 | ||||
| chr16:56625642-56625821 | Rare:53 | ||||
| chr16:56682232-56682568 | Common:6; Rare:113 | ||||
| chr16:56729967-56730185 | Common:1; Rare:49 | ||||
| chr16:56931915-56932168 | Common:3; Rare:125 | ||||
| chr16:57185755-57185800 | Rare:15 | ||||
| chr16:57185970-57186342 | Common:1; Rare:107 | ||||
| chr16:57447360-57447511 | Common:2; Rare:42; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:57619936-57620125 | Rare:42 | ||||
| chr16:57797930-57798268 | Rare:121 | ||||
| chr16:58001297-58001440 | Rare:38 |