| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:25673507-25673744 | Common:1; Rare:89 | ||||
| chr2:25878438-25878759 | Common:3; Rare:97 | ||||
| chr2:26244581-26244972 | Common:2; Rare:143; Clinvar:5; Clinvar (benign):9 | ||||
| chr2:26345785-26346184 | Common:1; Rare:120 | ||||
| chr2:26764183-26764325 | Common:1; Rare:56 | ||||
| chr2:26785807-26786107 | Rare:76 | ||||
| chr2:27032862-27032995 | Rare:50 | ||||
| chr2:27071604-27071872 | Common:1; Rare:83 | ||||
| chr2:27211722-27212146 | Common:3; Rare:144 | ||||
| chr2:27212225-27212413 | Common:2; Rare:103 | ||||
| chr2:27217218-27217489 | Rare:103 | ||||
| chr2:27323050-27323163 | Common:1; Rare:30; Clinvar (benign):1 | ||||
| chr2:27356743-27356854 | Rare:28 | ||||
| chr2:27356961-27357173 | Common:2; Rare:73 | ||||
| chr2:27370277-27370667 | Common:1; Rare:162 |