| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:26478990-26479280 | Common:2; Rare:68 | ||||
| chr22:26479402-26479827 | Common:3; Rare:146; Clinvar (benign):1 | ||||
| chr22:26479964-26480393 | Common:3; Rare:160 | ||||
| chr22:26483057-26483457 | Common:4; Rare:150 | ||||
| chr22:26483517-26484086 | Common:63; Rare:1047; Clinvar:43; Clinvar (benign):16 | ||||
| chr22:26512254-26512722 | Common:12; Rare:594 | ||||
| chr22:26589986-26590386 | Common:22; Rare:563 | ||||
| chr22:26617120-26617617 | Common:4; Rare:143 | ||||
| chr22:26617620-26618549 | Common:10; Rare:291; Clinvar:2 | ||||
| chr22:26618504-26618904 | Rare:79 | ||||
| chr22:27918600-27919071 | Common:5; Rare:417 | ||||
| chr22:27919145-27919577 | Common:35; Rare:1066 | ||||
| chr22:27919787-27920217 | Common:4; Rare:188 | ||||
| chr22:28442218-28442700 | Common:2; Rare:189 | ||||
| chr22:28442660-28442990 | Common:4; Rare:62 |