| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:58476018-58476213 | Common:2; Rare:66 | ||||
| chr19:58499068-58499675 | Common:5; Rare:222; Clinvar:10; Clinvar (benign):2 | ||||
| chr19:58519761-58520037 | Rare:72 | ||||
| chr19:58543983-58544096 | Rare:33 | ||||
| chr19:58544162-58544464 | Common:4; Rare:128 | ||||
| chr19:58554111-58554436 | Rare:91 | ||||
| chr19:58554939-58555223 | Common:2; Rare:94 | ||||
| chr19:58558276-58558675 | Rare:121 | ||||
| chr19:58558880-58559126 | Common:1; Rare:79 | ||||
| chr19:58573262-58573729 | Common:4; Rare:119 | ||||
| chr2:46885-47151 | Common:1; Rare:63 | ||||
| chr2:264012-264185 | Common:2; Rare:50 | ||||
| chr2:266870-267164 | Common:2; Rare:59 | ||||
| chr2:287126-287247 | Rare:20 | ||||
| chr2:287299-287359 | Rare:11 |