| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:19311997-19312333 | Common:8; Rare:161 | ||||
| chr1:20508107-20508187 | Common:1; Rare:29 | ||||
| chr1:20661359-20661702 | Common:3; Rare:124; Clinvar:4; Clinvar (benign):6 | ||||
| chr1:20786626-20786837 | Rare:81 | ||||
| chr1:20787230-20787445 | Rare:104 | ||||
| chr1:23368177-23368502 | Common:1; Rare:97 | ||||
| chr1:23558948-23559138 | Common:4; Rare:91 | ||||
| chr1:23559407-23559646 | Common:1; Rare:103 | ||||
| chr1:23778269-23778479 | Common:9; Rare:112 | ||||
| chr1:24642890-24643329 | Common:2; Rare:146 | ||||
| chr1:24745137-24745596 | Common:3; Rare:150 | ||||
| chr1:25232442-25232633 | Rare:77 | ||||
| chr1:25247445-25247640 | Common:2; Rare:70 | ||||
| chr1:25338242-25338510 | Common:2; Rare:90 | ||||
| chr1:25819805-25820013 | Common:4; Rare:66 |