| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:4704064-4704231 | Rare:91 | ||||
| chr17:4806990-4807216 | Common:4; Rare:70 | ||||
| chr17:4833259-4833523 | Rare:68 | ||||
| chr17:4939907-4940351 | Common:2; Rare:131 | ||||
| chr17:4942397-4942664 | Common:1; Rare:95 | ||||
| chr17:4948930-4949066 | Common:1; Rare:43 | ||||
| chr17:4950801-4951119 | Common:1; Rare:75; Clinvar (benign):1 | ||||
| chr17:4967793-4967951 | Rare:59 | ||||
| chr17:5078407-5078523 | Common:4; Rare:34 | ||||
| chr17:5123102-5123434 | Rare:108 | ||||
| chr17:5191832-5192054 | Common:1; Rare:71 | ||||
| chr17:5419556-5419869 | Common:3; Rare:111 | ||||
| chr17:5420142-5420213 | Rare:29 | ||||
| chr17:5468703-5468989 | Common:2; Rare:117 | ||||
| chr17:5486157-5486581 | Common:5; Rare:143 |