| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:26214535-26214856 | Common:1; Rare:57; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:26215108-26215285 | Rare:41 | ||||
| chr2:26244581-26245137 | Common:2; Rare:185; Clinvar:6; Clinvar (benign):9 | ||||
| chr2:26345783-26346165 | Common:1; Rare:116 | ||||
| chr2:26401842-26402013 | Common:3; Rare:51; Clinvar (benign):1 | ||||
| chr2:26562465-26562615 | Rare:40 | ||||
| chr2:26641324-26641427 | Rare:32 | ||||
| chr2:26764193-26764373 | Common:2; Rare:67 | ||||
| chr2:27014592-27014809 | Common:1; Rare:33 | ||||
| chr2:27032867-27033039 | Rare:62 | ||||
| chr2:27051461-27051786 | Rare:99 | ||||
| chr2:27071525-27071872 | Common:1; Rare:105 | ||||
| chr2:27078349-27078798 | Common:3; Rare:110 | ||||
| chr2:27086564-27086810 | Common:1; Rare:70; Clinvar (benign):1 | ||||
| chr2:27123731-27123865 | Common:2; Rare:30 |