| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:77412159-77412425 | Common:3; Rare:42 | ||||
| chr17:77413181-77413328 | Common:2; Rare:28 | ||||
| chr17:77413780-77413884 | Rare:17 | ||||
| chr17:77444272-77444498 | Common:1; Rare:35 | ||||
| chr17:77492640-77493073 | Common:2; Rare:103; Clinvar (benign):2 | ||||
| chr17:78108827-78108933 | Rare:15 | ||||
| chr17:78117269-78117549 | Rare:103; Clinvar:1 | ||||
| chr17:78537567-78537595 | Rare:7 | ||||
| chr17:78537604-78537754 | Common:1; Rare:29 | ||||
| chr17:78706288-78706360 | Rare:15 | ||||
| chr17:78787763-78787885 | Rare:23 | ||||
| chr17:79038613-79038927 | Common:6; Rare:43 | ||||
| chr17:80075469-80075631 | Rare:41 | ||||
| chr17:80222920-80222999 | Common:2; Rare:15 | ||||
| chr17:80336012-80336166 | Rare:41 |