| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:66437629-66437690 | Rare:18 | ||||
| chr2:66439166-66439343 | Common:1; Rare:34 | ||||
| chr2:66439867-66440136 | Common:5; Rare:94 | ||||
| chr2:66440339-66440611 | Common:1; Rare:50 | ||||
| chr2:66440744-66440915 | Common:2; Rare:46 | ||||
| chr2:67397263-67397450 | Rare:60 | ||||
| chr2:68062938-68063119 | Common:2; Rare:57 | ||||
| chr2:68157450-68157983 | Common:3; Rare:274 | ||||
| chr2:68252151-68252260 | Common:2; Rare:34 | ||||
| chr2:68252483-68252875 | Common:3; Rare:123 | ||||
| chr2:68467269-68467649 | Common:1; Rare:104 | ||||
| chr2:69387172-69387384 | Rare:54; Clinvar:2 | ||||
| chr2:69437395-69437696 | Common:1; Rare:143; Clinvar:6; Clinvar (benign):3 | ||||
| chr2:69643570-69643859 | Rare:99 | ||||
| chr2:69741984-69742164 | Common:1; Rare:44 |