| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:26112164-26112301 | Rare:36 | ||||
| chr1:26169773-26169988 | Common:4; Rare:67 | ||||
| chr1:26177288-26177618 | Common:4; Rare:95 | ||||
| chr1:26233896-26234263 | Common:3; Rare:113 | ||||
| chr1:26279810-26280120 | Rare:155 | ||||
| chr1:26306580-26306788 | Common:2; Rare:53 | ||||
| chr1:26336358-26336864 | Common:3; Rare:208 | ||||
| chr1:26354077-26354302 | Common:2; Rare:49 | ||||
| chr1:26432076-26432433 | Common:5; Rare:92; Clinvar:2; Clinvar (benign):1 | ||||
| chr1:26472289-26472453 | Common:4; Rare:47 | ||||
| chr1:26473023-26473244 | Common:1; Rare:119 | ||||
| chr1:26529477-26529801 | Common:3; Rare:96 | ||||
| chr1:26529956-26530356 | Common:6; Rare:112 | ||||
| chr1:26530980-26531230 | Rare:41 | ||||
| chr1:26531235-26531336 | Common:1; Rare:20 |