| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:27217304-27217545 | Rare:105 | ||||
| chr2:27323050-27323154 | Rare:25; Clinvar (benign):1 | ||||
| chr2:27356743-27357087 | Rare:96 | ||||
| chr2:27370310-27370677 | Common:1; Rare:145 | ||||
| chr2:27582948-27583122 | Rare:61 | ||||
| chr2:27628949-27629085 | Common:1; Rare:69 | ||||
| chr2:27663369-27663452 | Rare:25 | ||||
| chr2:27663490-27663941 | Rare:161 | ||||
| chr2:27771659-27772029 | Common:1; Rare:115 | ||||
| chr2:27890364-27890809 | Common:1; Rare:118 | ||||
| chr2:28751534-28752134 | Common:4; Rare:234 | ||||
| chr2:28870262-28870423 | Rare:63 | ||||
| chr2:28894354-28894745 | Common:5; Rare:143 | ||||
| chr2:30146600-30147016 | Common:5; Rare:134 | ||||
| chr2:30231269-30231555 | Common:1; Rare:88 |