| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:27118928-27119022 | Rare:20 | ||||
| chr2:27123731-27123892 | Common:2; Rare:39 | ||||
| chr2:27134553-27134907 | Common:1; Rare:137 | ||||
| chr2:27211379-27211422 | Rare:14 | ||||
| chr2:27211733-27212114 | Common:3; Rare:129 | ||||
| chr2:27212190-27212513 | Common:3; Rare:148 | ||||
| chr2:27212540-27212821 | Rare:58 | ||||
| chr2:27212956-27213053 | Rare:29 | ||||
| chr2:27216522-27216678 | Common:1; Rare:55 | ||||
| chr2:27217213-27217563 | Rare:140 | ||||
| chr2:27217900-27218136 | Common:2; Rare:75 | ||||
| chr2:27263006-27263207 | Rare:52 | ||||
| chr2:27264495-27264562 | Rare:15 | ||||
| chr2:27322934-27323395 | Common:4; Rare:137; Clinvar (benign):1 | ||||
| chr2:27323543-27323788 | Rare:47 |