| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:14069323-14069593 | Common:2; Rare:96; Clinvar:4; Clinvar (benign):3 | ||||
| chr17:14300821-14301167 | Common:3; Rare:94 | ||||
| chr17:15699514-15699768 | Common:3; Rare:66 | ||||
| chr17:15999598-16000028 | Common:3; Rare:184; Clinvar:6; Clinvar (benign):12; Clinvar (pathogenic):2 | ||||
| chr17:16039583-16039709 | Common:1; Rare:34 | ||||
| chr17:16040439-16040632 | Common:1; Rare:29 | ||||
| chr17:16046950-16047232 | Common:1; Rare:57 | ||||
| chr17:16215531-16215606 | Rare:29 | ||||
| chr17:17228197-17228304 | Rare:21 | ||||
| chr17:17591589-17591926 | Common:2; Rare:96 | ||||
| chr17:17851603-17851852 | Common:1; Rare:38 | ||||
| chr17:18039081-18039451 | Common:5; Rare:101; Clinvar:1; Clinvar (benign):1 | ||||
| chr17:18087838-18087997 | Rare:47 | ||||
| chr17:18183282-18183487 | Rare:47 | ||||
| chr17:18183751-18183931 | Rare:82 |