| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:26033778-26034167 | Common:3; Rare:142 | ||||
| chr2:26244582-26244984 | Common:2; Rare:148; Clinvar:5; Clinvar (benign):9 | ||||
| chr2:26345798-26346165 | Common:1; Rare:110 | ||||
| chr2:26764217-26764325 | Rare:42 | ||||
| chr2:27032841-27033001 | Rare:63 | ||||
| chr2:27051501-27051696 | Rare:58 | ||||
| chr2:27071515-27071872 | Common:1; Rare:106 | ||||
| chr2:27211742-27212103 | Common:3; Rare:123 | ||||
| chr2:27212261-27212398 | Common:2; Rare:74 | ||||
| chr2:27323043-27323154 | Rare:27; Clinvar (benign):1 | ||||
| chr2:27356750-27357199 | Common:2; Rare:136 | ||||
| chr2:27370259-27370648 | Common:1; Rare:160 | ||||
| chr2:27442353-27442423 | Rare:38 | ||||
| chr2:27489643-27489970 | Common:1; Rare:87; Clinvar (benign):1 | ||||
| chr2:27582797-27583122 | Rare:109 |