| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:27086582-27086797 | Common:1; Rare:62; Clinvar (benign):1 | ||||
| chr2:27211794-27212109 | Common:3; Rare:106 | ||||
| chr2:27212223-27212467 | Common:2; Rare:125 | ||||
| chr2:27323049-27323154 | Rare:25; Clinvar (benign):1 | ||||
| chr2:27356177-27356293 | Rare:28 | ||||
| chr2:27356743-27356855 | Rare:29 | ||||
| chr2:27356970-27357199 | Common:2; Rare:84 | ||||
| chr2:27370275-27370646 | Common:1; Rare:153 | ||||
| chr2:27380774-27380962 | Common:1; Rare:64 | ||||
| chr2:27443198-27443443 | Rare:72 | ||||
| chr2:27489647-27489950 | Rare:77; Clinvar (benign):1 | ||||
| chr2:27582997-27583101 | Rare:40 | ||||
| chr2:27628949-27629058 | Common:1; Rare:53 | ||||
| chr2:27663351-27663467 | Rare:32 | ||||
| chr2:27663516-27663934 | Rare:150 |