| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:105487118-105487297 | Common:2; Rare:67 | ||||
| chr14:105488161-105488493 | Common:6; Rare:149 | ||||
| chr14:105488512-105488668 | Common:1; Rare:51 | ||||
| chr14:105489884-105490228 | Common:4; Rare:96 | ||||
| chr15:22786479-22786816 | Rare:117; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr15:22838464-22838930 | Common:4; Rare:157 | ||||
| chr15:23039059-23039178 | Common:1; Rare:28 | ||||
| chr15:23039439-23039698 | Common:1; Rare:116 | ||||
| chr15:26615378-26615695 | Common:1; Rare:62 | ||||
| chr15:26772441-26772759 | Rare:96; Clinvar (benign):4 | ||||
| chr15:26866677-26866788 | Common:1; Rare:20 | ||||
| chr15:26866921-26867370 | Common:3; Rare:129 | ||||
| chr15:28886049-28886238 | Common:1; Rare:58 | ||||
| chr15:29822005-29822242 | Rare:88 | ||||
| chr15:29822408-29822586 | Common:1; Rare:71 |