| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:69387183-69387398 | Rare:58; Clinvar:2 | ||||
| chr2:69643591-69643824 | Rare:79 | ||||
| chr2:69914767-69915096 | Common:1; Rare:76 | ||||
| chr2:70086931-70087116 | Common:1; Rare:93 | ||||
| chr2:70087307-70087750 | Common:2; Rare:172 | ||||
| chr2:70087756-70088089 | Rare:81 | ||||
| chr2:70258017-70258242 | Common:2; Rare:78 | ||||
| chr2:70553820-70553861 | Common:1; Rare:12 | ||||
| chr2:71068526-71068686 | Rare:75 | ||||
| chr2:71129805-71129908 | Rare:19 | ||||
| chr2:71130224-71130327 | Common:1; Rare:41; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:73071701-73071848 | Common:2; Rare:57 | ||||
| chr2:73234119-73234383 | Common:2; Rare:72 | ||||
| chr2:73385620-73385860 | Common:2; Rare:93; Clinvar:6; Clinvar (benign):3 | ||||
| chr2:73828910-73829020 | Rare:32 |