| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:8152348-8152559 | Common:2; Rare:48 | ||||
| chr17:8162886-8163093 | Rare:72 | ||||
| chr17:8190210-8190502 | Common:1; Rare:78 | ||||
| chr17:8248032-8248110 | Common:2; Rare:44; Clinvar:2; Clinvar (benign):2 | ||||
| chr17:8376671-8376766 | Common:1; Rare:35 | ||||
| chr17:8965684-8965777 | Common:1; Rare:29 | ||||
| chr17:10697485-10697654 | Common:3; Rare:75; Clinvar:5; Clinvar (benign):2 | ||||
| chr17:10729667-10729818 | Rare:66 | ||||
| chr17:10729925-10730045 | Common:4; Rare:33 | ||||
| chr17:14069335-14069580 | Common:2; Rare:87; Clinvar:3; Clinvar (benign):3 | ||||
| chr17:14300806-14301099 | Common:2; Rare:78 | ||||
| chr17:15699510-15699768 | Common:3; Rare:67 | ||||
| chr17:15999605-16000028 | Common:3; Rare:180; Clinvar:6; Clinvar (benign):12; Clinvar (pathogenic):2 | ||||
| chr17:16039730-16039769 | Rare:6 | ||||
| chr17:16380826-16381182 | Common:3; Rare:125 |