| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:56669708-56669871 | Rare:31 | ||||
| chr16:56682077-56682568 | Common:8; Rare:142 | ||||
| chr16:56730012-56730211 | Common:1; Rare:48 | ||||
| chr16:56740859-56740967 | Common:1; Rare:5 | ||||
| chr16:56931840-56932175 | Common:3; Rare:146 | ||||
| chr16:56989371-56989605 | Common:1; Rare:55; Clinvar:1 | ||||
| chr16:57145887-57146205 | Rare:74 | ||||
| chr16:57185346-57185410 | Rare:11 | ||||
| chr16:57185711-57186429 | Common:4; Rare:202 | ||||
| chr16:57245020-57245356 | Common:3; Rare:117 | ||||
| chr16:57372311-57372492 | Rare:39 | ||||
| chr16:57447344-57447525 | Common:2; Rare:56; Clinvar:2; Clinvar (benign):2 | ||||
| chr16:57619573-57619782 | Common:2; Rare:44 | ||||
| chr16:57619942-57620128 | Rare:42 | ||||
| chr16:57797863-57798140 | Rare:82 |