| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:7573099-7574000 | Common:10; Rare:495 | ||||
| chr17:7577057-7577358 | Common:1; Rare:77 | ||||
| chr17:7579364-7581419 | Common:11; Rare:1367 | ||||
| chr17:7583495-7583986 | Common:7; Rare:897; Clinvar:22; Clinvar (benign):27; Clinvar (pathogenic):5 | ||||
| chr17:7583909-7584866 | Common:2; Rare:404 | ||||
| chr17:7585599-7586044 | Rare:199; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):4 | ||||
| chr17:7586694-7587094 | Common:2; Rare:144; Clinvar:3; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr17:7613747-7614147 | Common:2; Rare:100 | ||||
| chr17:7614343-7614450 | Rare:24 | ||||
| chr17:7614548-7614710 | Rare:99 | ||||
| chr17:7614704-7615488 | Rare:861 | ||||
| chr17:7627722-7628122 | Common:9; Rare:317 | ||||
| chr17:7650491-7650960 | Common:12; Rare:572 | ||||
| chr17:7685256-7685656 | Common:3; Rare:65 | ||||
| chr17:7685960-7686728 | Common:1; Rare:607 |