| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:109613562-109613827 | Common:3; Rare:76 | ||||
| chr2:109613833-109614460 | Common:6; Rare:223 | ||||
| chr2:110115796-110115965 | Common:2; Rare:41 | ||||
| chr2:110204857-110205131 | Common:1; Rare:112; Clinvar:4; Clinvar (benign):1 | ||||
| chr2:110212062-110212106 | Rare:7 | ||||
| chr2:110212281-110212350 | Common:2; Rare:20 | ||||
| chr2:110212443-110212646 | Common:1; Rare:53 | ||||
| chr2:110677955-110678292 | Rare:118 | ||||
| chr2:110678574-110678731 | Rare:21 | ||||
| chr2:110732451-110732669 | Common:1; Rare:69 | ||||
| chr2:111120242-111120957 | Common:6; Rare:250 | ||||
| chr2:111122398-111122761 | Common:3; Rare:150 | ||||
| chr2:111122777-111122941 | Rare:60 | ||||
| chr2:111123063-111123139 | Rare:28 | ||||
| chr2:111123172-111123301 | Rare:47 |