| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:58219216-58219348 | Common:1; Rare:50; Clinvar:2; Clinvar (benign):4 | ||||
| chr17:58328563-58328952 | Common:2; Rare:81 | ||||
| chr17:58352130-58352466 | Common:6; Rare:133 | ||||
| chr17:58517831-58518068 | Common:1; Rare:54 | ||||
| chr17:58692513-58692673 | Common:2; Rare:90; Clinvar:12; Clinvar (benign):20 | ||||
| chr17:59106699-59107025 | Common:2; Rare:110; Clinvar:4; Clinvar (benign):2 | ||||
| chr17:59154982-59155781 | Common:2; Rare:215 | ||||
| chr17:59220394-59220649 | Common:3; Rare:76 | ||||
| chr17:59331477-59331756 | Common:2; Rare:91 | ||||
| chr17:59565488-59565674 | Rare:75 | ||||
| chr17:59619557-59619983 | Common:3; Rare:152 | ||||
| chr17:59655679-59655895 | Rare:37 | ||||
| chr17:59685430-59685662 | Common:1; Rare:44 | ||||
| chr17:59707397-59707539 | Common:1; Rare:35; Clinvar (benign):3 | ||||
| chr17:59707597-59707732 | Common:2; Rare:39 |