| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:52553442-52553565 | Common:2; Rare:37 | ||||
| chr1:52698078-52698120 | Rare:9 | ||||
| chr1:52698318-52698464 | Common:2; Rare:50 | ||||
| chr1:52927219-52927317 | Common:1; Rare:30 | ||||
| chr1:53220545-53220703 | Common:1; Rare:81 | ||||
| chr1:53238444-53238592 | Rare:66 | ||||
| chr1:53238599-53238713 | Rare:32 | ||||
| chr1:53327875-53328248 | Common:2; Rare:97 | ||||
| chr1:53889765-53889974 | Common:2; Rare:64 | ||||
| chr1:53945562-53946055 | Common:8; Rare:127 | ||||
| chr1:53946253-53946459 | Rare:76 | ||||
| chr1:54053145-54053637 | Common:6; Rare:165 | ||||
| chr1:54199985-54200259 | Rare:81 | ||||
| chr1:54764531-54764845 | Common:6; Rare:89 | ||||
| chr1:54887128-54887398 | Common:1; Rare:93; Clinvar:4; Clinvar (benign):1 |