| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:229342354-229342742 | Rare:124 | ||||
| chr1:229343009-229343153 | Common:1; Rare:32 | ||||
| chr1:229343231-229343471 | Common:1; Rare:56 | ||||
| chr1:229507995-229508537 | Common:2; Rare:215 | ||||
| chr1:229558075-229558265 | Common:3; Rare:66 | ||||
| chr1:229558986-229559263 | Common:1; Rare:84 | ||||
| chr1:229625618-229625770 | Rare:35 | ||||
| chr1:229626054-229626540 | Common:4; Rare:148 | ||||
| chr1:229626719-229626745 | Rare:4 | ||||
| chr1:230066600-230066877 | Common:2; Rare:59 | ||||
| chr1:230066972-230067290 | Common:1; Rare:133 | ||||
| chr1:230642287-230642593 | Common:1; Rare:110 | ||||
| chr1:230642697-230642844 | Common:1; Rare:51 | ||||
| chr1:230868483-230868622 | Rare:47 | ||||
| chr1:230978715-230979206 | Common:4; Rare:186; Clinvar (benign):1 |