| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:108719294-108719553 | Common:2; Rare:112 | ||||
| chr2:108786636-108786855 | Common:7; Rare:121 | ||||
| chr2:109613017-109613667 | Common:6; Rare:259 | ||||
| chr2:109614084-109614404 | Common:4; Rare:118 | ||||
| chr2:110204911-110205109 | Common:1; Rare:88; Clinvar:3; Clinvar (benign):1 | ||||
| chr2:110212513-110212658 | Rare:36 | ||||
| chr2:110678055-110678270 | Rare:63 | ||||
| chr2:111120685-111120945 | Common:2; Rare:116 | ||||
| chr2:111122401-111122681 | Common:2; Rare:118 | ||||
| chr2:111884095-111884331 | Common:1; Rare:75 | ||||
| chr2:111898269-111898676 | Common:2; Rare:96 | ||||
| chr2:112055649-112056092 | Common:4; Rare:266 | ||||
| chr2:112254718-112254841 | Rare:28 | ||||
| chr2:112254995-112255207 | Common:2; Rare:89 | ||||
| chr2:112275304-112275670 | Common:1; Rare:132 |