| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:53838433-53838526 | Rare:23 | ||||
| chr1:53889765-53889977 | Common:2; Rare:66 | ||||
| chr1:53945553-53946045 | Common:7; Rare:121 | ||||
| chr1:53946260-53946501 | Common:1; Rare:85 | ||||
| chr1:54053172-54053806 | Common:6; Rare:201 | ||||
| chr1:54199982-54200214 | Rare:54 | ||||
| chr1:54542093-54542284 | Common:2; Rare:56 | ||||
| chr1:54547973-54548238 | Common:1; Rare:57 | ||||
| chr1:54715720-54715905 | Common:3; Rare:57 | ||||
| chr1:54764477-54764845 | Common:7; Rare:108 | ||||
| chr1:54887128-54887431 | Common:3; Rare:104; Clinvar:4; Clinvar (benign):1 | ||||
| chr1:55214639-55214729 | Common:1; Rare:27 | ||||
| chr1:56645009-56645387 | Common:1; Rare:125 | ||||
| chr1:58546706-58546828 | Common:4; Rare:59 | ||||
| chr1:58700048-58700167 | Common:4; Rare:51 |