| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:16380990-16381155 | Common:1; Rare:77 | ||||
| chr17:16415455-16415825 | Common:4; Rare:85 | ||||
| chr17:16419245-16419350 | Rare:27 | ||||
| chr17:16419571-16419806 | Common:1; Rare:48 | ||||
| chr17:16569067-16569384 | Common:2; Rare:93 | ||||
| chr17:16569538-16569740 | Common:1; Rare:52 | ||||
| chr17:16653539-16653604 | Rare:21 | ||||
| chr17:16653613-16653675 | Common:1; Rare:20 | ||||
| chr17:16653699-16653877 | Common:1; Rare:55 | ||||
| chr17:16971502-16971801 | Common:4; Rare:43 | ||||
| chr17:16971883-16972364 | Common:1; Rare:127; Clinvar:2; Clinvar (benign):2 | ||||
| chr17:17042092-17042568 | Common:20; Rare:158 | ||||
| chr17:17206261-17206605 | Common:4; Rare:132 | ||||
| chr17:17237087-17237231 | Common:1; Rare:55; Clinvar:1; Clinvar (benign):3 | ||||
| chr17:17237309-17237884 | Common:8; Rare:145 |