| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:31346572-31346768 | Common:5; Rare:33 | ||||
| chr22:31399363-31399658 | Common:1; Rare:84 | ||||
| chr22:31496409-31496556 | Common:1; Rare:37 | ||||
| chr22:31630829-31630961 | Common:3; Rare:35 | ||||
| chr22:31662181-31662368 | Common:2; Rare:79 | ||||
| chr22:31750031-31750216 | Common:3; Rare:66 | ||||
| chr22:31753792-31754098 | Common:1; Rare:109 | ||||
| chr22:32412169-32412315 | Common:2; Rare:44 | ||||
| chr22:35257367-35257520 | Common:1; Rare:37 | ||||
| chr22:35299634-35299931 | Common:3; Rare:79 | ||||
| chr22:35399903-35400183 | Rare:99 | ||||
| chr22:35961576-35961907 | Common:1; Rare:59 | ||||
| chr22:36239512-36239671 | Rare:50 | ||||
| chr22:36387981-36388322 | Common:2; Rare:94; Clinvar (benign):1 | ||||
| chr22:36481604-36481734 | Common:2; Rare:33 |