| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:81666554-81666763 | Common:1; Rare:91 | ||||
| chr17:81683721-81684057 | Common:4; Rare:167 | ||||
| chr17:81703294-81703488 | Common:2; Rare:53; Clinvar (benign):2 | ||||
| chr17:81937180-81937441 | Rare:97 | ||||
| chr17:82037683-82037856 | Common:1; Rare:67 | ||||
| chr17:82051619-82051948 | Common:2; Rare:95 | ||||
| chr17:82273412-82273812 | Common:1; Rare:138 | ||||
| chr17:82450716-82450893 | Common:2; Rare:69 | ||||
| chr17:82458517-82458771 | Common:3; Rare:90 | ||||
| chr17:82716455-82716750 | Common:6; Rare:104 | ||||
| chr18:268023-268113 | Common:1; Rare:28 | ||||
| chr18:658312-658414 | Common:1; Rare:19 | ||||
| chr18:812191-812437 | Common:3; Rare:85 | ||||
| chr18:812741-812794 | Rare:18 | ||||
| chr18:2571493-2571611 | Rare:30 |