| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:64653721-64654089 | Common:1; Rare:138 | ||||
| chr2:64988341-64988498 | Common:1; Rare:30 | ||||
| chr2:64989091-64989426 | Common:7; Rare:85 | ||||
| chr2:65056149-65056462 | Common:2; Rare:107 | ||||
| chr2:65227582-65227955 | Rare:100 | ||||
| chr2:66434805-66435299 | Common:2; Rare:117 | ||||
| chr2:66440345-66440570 | Common:1; Rare:44 | ||||
| chr2:68062960-68063119 | Common:2; Rare:51 | ||||
| chr2:68157456-68157955 | Common:2; Rare:256 | ||||
| chr2:68251557-68251623 | Common:1; Rare:19 | ||||
| chr2:68252144-68252331 | Common:2; Rare:62 | ||||
| chr2:68252470-68252868 | Common:3; Rare:129 | ||||
| chr2:68467214-68467649 | Common:2; Rare:121 | ||||
| chr2:69387172-69387398 | Rare:60; Clinvar:2 | ||||
| chr2:69437428-69437665 | Common:1; Rare:113; Clinvar:6; Clinvar (benign):2 |