| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:58440148-58440398 | Common:5; Rare:67 | ||||
| chr19:58476018-58476169 | Common:1; Rare:55 | ||||
| chr19:58499211-58499530 | Common:2; Rare:97; Clinvar:3 | ||||
| chr19:58519786-58519814 | Rare:7 | ||||
| chr19:58558955-58559167 | Common:1; Rare:65 | ||||
| chr19:58573298-58573645 | Common:2; Rare:84 | ||||
| chr2:264561-264991 | Common:4; Rare:165 | ||||
| chr2:677358-677517 | Common:1; Rare:62 | ||||
| chr2:3379646-3379807 | Common:2; Rare:68 | ||||
| chr2:3519478-3519660 | Common:2; Rare:57 | ||||
| chr2:3558251-3558489 | Common:5; Rare:104 | ||||
| chr2:3575107-3575447 | Common:2; Rare:98; Clinvar:3; Clinvar (benign):6 | ||||
| chr2:9423148-9423676 | Common:1; Rare:139 | ||||
| chr2:9473684-9473776 | Rare:24 | ||||
| chr2:9474498-9474627 | Common:6; Rare:61 |