| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:11980104-11980478 | Common:6; Rare:121; Clinvar:1; Clinvar (benign):5 | ||||
| chr1:12464784-12464960 | Rare:28 | ||||
| chr1:12616619-12616854 | Common:1; Rare:45 | ||||
| chr1:12617163-12617584 | Rare:107 | ||||
| chr1:12617585-12617612 | Rare:3 | ||||
| chr1:12617641-12618475 | Common:9; Rare:149 | ||||
| chr1:13749066-13749464 | Common:2; Rare:133 | ||||
| chr1:15409782-15409902 | Common:1; Rare:38 | ||||
| chr1:15524242-15524569 | Common:2; Rare:81 | ||||
| chr1:15526553-15526917 | Common:2; Rare:117 | ||||
| chr1:16017385-16017747 | Common:1; Rare:87 | ||||
| chr1:16017833-16018239 | Common:9; Rare:146 | ||||
| chr1:16352410-16352655 | Common:4; Rare:123 | ||||
| chr1:16455580-16455892 | Common:1; Rare:70 | ||||
| chr1:17053960-17054316 | Common:3; Rare:116; Clinvar:16; Clinvar (benign):10 |