| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:105487729-105487974 | Rare:75 | ||||
| chr14:105489613-105489951 | Common:2; Rare:62 | ||||
| chr14:105490016-105490126 | Common:1; Rare:37 | ||||
| chr14:105490617-105491401 | Common:1; Rare:225 | ||||
| chr14:105491627-105491723 | Common:1; Rare:44 | ||||
| chr14:105526415-105526615 | Common:2; Rare:47 | ||||
| chr14:105528490-105528597 | Rare:22 | ||||
| chr15:22786153-22786872 | Common:3; Rare:224; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr15:22787084-22787341 | Common:3; Rare:62 | ||||
| chr15:22838189-22838253 | Rare:12 | ||||
| chr15:22838333-22838818 | Common:4; Rare:164 | ||||
| chr15:22979699-22979955 | Common:1; Rare:74 | ||||
| chr15:22980117-22980595 | Common:5; Rare:174 | ||||
| chr15:22980696-22980927 | Common:3; Rare:94 | ||||
| chr15:22980938-22981104 | Common:1; Rare:33 |