| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:31489117-31490526 | Common:26; Rare:1481 | ||||
| chr22:31495850-31496294 | Common:7; Rare:346 | ||||
| chr22:31496245-31496740 | Common:13; Rare:452 | ||||
| chr22:31583922-31584322 | Common:2; Rare:82 | ||||
| chr22:31625634-31626034 | Common:5; Rare:249; Clinvar (benign):1 | ||||
| chr22:31626570-31627089 | Common:18; Rare:286 | ||||
| chr22:31629491-31629891 | Common:6; Rare:141 | ||||
| chr22:31630240-31630710 | Common:3; Rare:277 | ||||
| chr22:31630730-31631130 | Common:38; Rare:454 | ||||
| chr22:31661780-31662060 | Common:4; Rare:129 | ||||
| chr22:31662101-31662501 | Common:9; Rare:455 | ||||
| chr22:31749310-31749772 | Common:1; Rare:166 | ||||
| chr22:31749940-31750399 | Common:18; Rare:582 | ||||
| chr22:31753208-31753608 | Rare:78 | ||||
| chr22:31753617-31754146 | Common:7; Rare:850 |