| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:81761197-81761342 | Rare:54 | ||||
| chr3:81761530-81761600 | Common:5; Rare:22; Clinvar (benign):1 | ||||
| chr3:84960632-84960897 | Common:2; Rare:54 | ||||
| chr3:84962294-84962604 | Common:3; Rare:50 | ||||
| chr3:84984161-84984394 | Common:2; Rare:44 | ||||
| chr3:87227950-87227975 | Rare:4 | ||||
| chr3:90072896-90072971 | Common:2; Rare:15 | ||||
| chr3:98191243-98191359 | Common:1; Rare:31 | ||||
| chr3:98193970-98194185 | Common:6; Rare:44 | ||||
| chr3:98325135-98325345 | Common:3; Rare:40 | ||||
| chr3:101576879-101576966 | Common:1; Rare:24 | ||||
| chr3:101676157-101676507 | Common:6; Rare:105 | ||||
| chr3:104444388-104444558 | Common:3; Rare:27 | ||||
| chr3:105403982-105404130 | Rare:25 | ||||
| chr3:106831167-106831222 | Rare:11 |