| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:8435726-8436006 | Common:4; Rare:111 | ||||
| chr17:8965678-8965783 | Common:1; Rare:34 | ||||
| chr17:9576602-9576676 | Rare:16 | ||||
| chr17:10697503-10697654 | Common:3; Rare:59; Clinvar:2; Clinvar (benign):2 | ||||
| chr17:10729974-10730111 | Common:3; Rare:33 | ||||
| chr17:13018016-13018333 | Common:6; Rare:91 | ||||
| chr17:14069440-14069580 | Common:2; Rare:57; Clinvar:3; Clinvar (benign):3 | ||||
| chr17:15260791-15261033 | Common:2; Rare:75; Clinvar (benign):1 | ||||
| chr17:15999554-16000025 | Common:3; Rare:199; Clinvar:6; Clinvar (benign):12; Clinvar (pathogenic):2 | ||||
| chr17:16039597-16039720 | Common:1; Rare:32 | ||||
| chr17:16215544-16215639 | Common:1; Rare:43 | ||||
| chr17:16380564-16380820 | Common:4; Rare:67 | ||||
| chr17:16689997-16690269 | Common:3; Rare:59 | ||||
| chr17:17237133-17237429 | Common:4; Rare:89; Clinvar (benign):2 | ||||
| chr17:17281158-17281365 | Rare:80 |