| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:42388392-42388765 | Rare:109; Clinvar:3 | ||||
| chr17:42423248-42423445 | Common:1; Rare:50 | ||||
| chr17:42458730-42458914 | Common:1; Rare:71 | ||||
| chr17:42566985-42567151 | Common:3; Rare:52 | ||||
| chr17:42577541-42577864 | Common:1; Rare:148 | ||||
| chr17:42609320-42609732 | Common:8; Rare:173; Clinvar (benign):2 | ||||
| chr17:42659164-42659396 | Rare:76 | ||||
| chr17:42773355-42773475 | Rare:34 | ||||
| chr17:42833196-42833506 | Rare:94 | ||||
| chr17:42964423-42964536 | Rare:52 | ||||
| chr17:43125313-43125654 | Rare:90; Clinvar:3; Clinvar (benign):3 | ||||
| chr17:43171043-43171249 | Rare:62 | ||||
| chr17:43544986-43545053 | Common:1; Rare:14 | ||||
| chr17:43545601-43545778 | Common:1; Rare:53 | ||||
| chr17:43778894-43779062 | Rare:40 |