| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:56682276-56682513 | Common:4; Rare:81 | ||||
| chr16:56729949-56730189 | Common:1; Rare:58 | ||||
| chr16:56781577-56781866 | Common:1; Rare:53 | ||||
| chr16:56931975-56932177 | Common:2; Rare:113 | ||||
| chr16:56989392-56989574 | Common:1; Rare:40; Clinvar:1 | ||||
| chr16:57185746-57186377 | Common:3; Rare:179 | ||||
| chr16:57244959-57245339 | Common:3; Rare:126 | ||||
| chr16:57372306-57372579 | Rare:69 | ||||
| chr16:57447360-57447536 | Common:2; Rare:54; Clinvar:2; Clinvar (benign):3 | ||||
| chr16:57628380-57628418 | Common:1; Rare:4 | ||||
| chr16:57628520-57628699 | Common:3; Rare:45 | ||||
| chr16:57639169-57639506 | Common:1; Rare:63; Clinvar (pathogenic):1 | ||||
| chr16:57803220-57803413 | Rare:36 | ||||
| chr16:58001245-58001458 | Common:1; Rare:52 | ||||
| chr16:58129132-58129576 | Common:7; Rare:133 |