| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:81916782-81916898 | Rare:25 | ||||
| chr17:81917413-81918148 | Common:3; Rare:414 | ||||
| chr17:81922637-81923418 | Common:4; Rare:250 | ||||
| chr17:81923344-81923788 | Common:20; Rare:441 | ||||
| chr17:81926823-81927223 | Rare:110 | ||||
| chr17:81927531-81928039 | Common:6; Rare:603 | ||||
| chr17:81928112-81928520 | Common:1; Rare:159 | ||||
| chr17:81936359-81936998 | Common:3; Rare:205; Clinvar:2; Clinvar (benign):5; Clinvar (pathogenic):2 | ||||
| chr17:81937058-81937652 | Rare:823 | ||||
| chr17:81959260-81959540 | Common:2; Rare:106 | ||||
| chr17:81959623-81960474 | Common:16; Rare:650 | ||||
| chr17:81960488-81960646 | Rare:58 | ||||
| chr17:81961219-81961707 | Common:13; Rare:465 | ||||
| chr17:81976548-81977081 | Common:5; Rare:142 | ||||
| chr17:81977325-81977725 | Rare:644 |