| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:4968688-4968766 | Rare:24 | ||||
| chr17:4969247-4969572 | Rare:94 | ||||
| chr17:4969630-4969643 | Rare:5 | ||||
| chr17:4987404-4987601 | Common:2; Rare:52 | ||||
| chr17:4987629-4987833 | Common:2; Rare:67 | ||||
| chr17:4997479-4997751 | Common:2; Rare:100 | ||||
| chr17:4997848-4998303 | Common:4; Rare:161; Clinvar (benign):3 | ||||
| chr17:5077832-5078034 | Common:2; Rare:34 | ||||
| chr17:5078084-5078306 | Common:1; Rare:55 | ||||
| chr17:5078311-5078600 | Common:4; Rare:69 | ||||
| chr17:5111784-5112119 | Common:6; Rare:107 | ||||
| chr17:5123065-5123207 | Rare:41 | ||||
| chr17:5191785-5192149 | Common:2; Rare:113 | ||||
| chr17:5282021-5282334 | Common:13; Rare:157 | ||||
| chr17:5419605-5419951 | Common:6; Rare:106 |