| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:26847893-26848207 | Common:2; Rare:89 | ||||
| chr2:27032805-27032983 | Rare:64 | ||||
| chr2:27051546-27051706 | Rare:49 | ||||
| chr2:27071551-27071893 | Common:1; Rare:102 | ||||
| chr2:27078396-27078730 | Common:3; Rare:83 | ||||
| chr2:27211710-27212072 | Common:3; Rare:121 | ||||
| chr2:27212229-27212387 | Common:2; Rare:85 | ||||
| chr2:27217317-27217544 | Rare:101 | ||||
| chr2:27323043-27323163 | Common:1; Rare:32; Clinvar (benign):1 | ||||
| chr2:27356177-27356286 | Rare:26 | ||||
| chr2:27356738-27356913 | Rare:42 | ||||
| chr2:27356973-27357170 | Common:2; Rare:67 | ||||
| chr2:27370247-27370641 | Common:1; Rare:160 | ||||
| chr2:27380396-27380655 | Common:1; Rare:94; Clinvar:5 | ||||
| chr2:27489689-27489953 | Rare:63; Clinvar (benign):1 |