| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:108448861-108449317 | Common:2; Rare:161 | ||||
| chr2:108533782-108534575 | Common:10; Rare:281 | ||||
| chr2:108534758-108534895 | Rare:40 | ||||
| chr2:108621188-108621251 | Rare:6 | ||||
| chr2:108719314-108719571 | Common:3; Rare:112; Clinvar (benign):2 | ||||
| chr2:108719717-108719826 | Rare:35 | ||||
| chr2:108786568-108786854 | Common:7; Rare:135 | ||||
| chr2:109129014-109129260 | Rare:106 | ||||
| chr2:109613607-109613799 | Common:2; Rare:50 | ||||
| chr2:109613875-109613990 | Common:1; Rare:39 | ||||
| chr2:109614114-109614351 | Common:3; Rare:81 | ||||
| chr2:110204950-110205135 | Common:1; Rare:74; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:110212265-110212706 | Common:4; Rare:110 | ||||
| chr2:110677790-110677862 | Rare:13 | ||||
| chr2:110677986-110678292 | Rare:107 |