| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:3443481-3443715 | Common:3; Rare:78 | ||||
| chr16:3457833-3458131 | Common:3; Rare:138 | ||||
| chr16:3611554-3611766 | Rare:85; Clinvar:1 | ||||
| chr16:4425750-4425879 | Common:1; Rare:61 | ||||
| chr16:4476306-4476448 | Common:1; Rare:55 | ||||
| chr16:4538394-4538614 | Common:2; Rare:74 | ||||
| chr16:4767126-4767392 | Common:1; Rare:85 | ||||
| chr16:5033933-5033987 | Rare:20 | ||||
| chr16:8621612-8621733 | Common:1; Rare:48 | ||||
| chr16:8797631-8797866 | Rare:88; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:8868983-8869227 | Common:4; Rare:111 | ||||
| chr16:10743726-10743855 | Rare:50 | ||||
| chr16:10944327-10944582 | Common:1; Rare:75 | ||||
| chr16:11345210-11345451 | Common:1; Rare:75 | ||||
| chr16:11797196-11797527 | Common:2; Rare:125 |