| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:19977834-19977960 | Common:1; Rare:42 | ||||
| chr17:20155878-20156103 | Common:1; Rare:77 | ||||
| chr17:21214140-21214344 | Common:2; Rare:89 | ||||
| chr17:28335368-28335824 | Common:1; Rare:109 | ||||
| chr17:28357451-28357679 | Common:5; Rare:115 | ||||
| chr17:28661873-28661950 | Rare:35 | ||||
| chr17:28662102-28662288 | Rare:78 | ||||
| chr17:28717832-28717998 | Rare:36 | ||||
| chr17:29568473-29568740 | Common:4; Rare:88 | ||||
| chr17:30906203-30906327 | Common:1; Rare:38 | ||||
| chr17:32350041-32350185 | Rare:74 | ||||
| chr17:34961495-34961540 | Rare:17 | ||||
| chr17:35242906-35243133 | Rare:78 | ||||
| chr17:35373618-35373841 | Common:4; Rare:44 | ||||
| chr17:35578539-35578684 | Common:1; Rare:33; Clinvar (benign):1 |