| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:49724231-49724303 | Rare:19 | ||||
| chr22:49874005-49874135 | Common:1; Rare:30 | ||||
| chr22:50019425-50019564 | Rare:19 | ||||
| chr22:50152451-50152626 | Common:1; Rare:32 | ||||
| chr22:50207581-50207772 | Rare:46 | ||||
| chr22:50267665-50267833 | Common:1; Rare:68 | ||||
| chr22:50271771-50271872 | Rare:33 | ||||
| chr22:50448598-50448685 | Rare:26 | ||||
| chr22:50459255-50459598 | Common:4; Rare:158; Clinvar:4; Clinvar (benign):1 | ||||
| chr22:50464384-50464652 | Common:1; Rare:112; Clinvar:1 | ||||
| chr22:50574112-50574275 | Rare:42 | ||||
| chr22:50725164-50725302 | Rare:30 | ||||
| chr22:50807055-50807311 | Rare:17 | ||||
| chr3:535654-535902 | Common:1; Rare:66 | ||||
| chr3:535959-536273 | Common:3; Rare:119 |