| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:69387125-69387398 | Rare:74; Clinvar:2 | ||||
| chr2:69643591-69643825 | Rare:80 | ||||
| chr2:70087307-70087762 | Common:2; Rare:177 | ||||
| chr2:70190980-70191142 | Common:1; Rare:42 | ||||
| chr2:70258022-70258168 | Common:1; Rare:50 | ||||
| chr2:70293659-70293821 | Common:2; Rare:58 | ||||
| chr2:71068538-71068663 | Rare:56 | ||||
| chr2:71129812-71129891 | Rare:15 | ||||
| chr2:71130194-71130662 | Common:6; Rare:133; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:71453283-71453686 | Common:1; Rare:66 | ||||
| chr2:71453688-71453871 | Common:2; Rare:29 | ||||
| chr2:73071706-73071863 | Common:2; Rare:57 | ||||
| chr2:73828800-73829029 | Common:1; Rare:53 | ||||
| chr2:74002570-74002738 | Common:2; Rare:69 | ||||
| chr2:74147870-74148140 | Common:1; Rare:66; Clinvar:2 |