| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:44648543-44648791 | Rare:50 | ||||
| chr3:44729435-44729706 | Common:4; Rare:99 | ||||
| chr3:44761585-44761927 | Common:3; Rare:123 | ||||
| chr3:44761970-44762144 | Rare:31 | ||||
| chr3:44861713-44861999 | Common:4; Rare:117 | ||||
| chr3:44976066-44976350 | Common:3; Rare:117 | ||||
| chr3:44976672-44976694 | Rare:4 | ||||
| chr3:45146292-45146557 | Common:1; Rare:95 | ||||
| chr3:45388394-45388712 | Common:3; Rare:88; Clinvar (benign):1 | ||||
| chr3:45388808-45388836 | Rare:3 | ||||
| chr3:45593732-45594308 | Common:7; Rare:162 | ||||
| chr3:45688819-45689063 | Common:3; Rare:127 | ||||
| chr3:45689073-45689471 | Common:3; Rare:148 | ||||
| chr3:45842066-45842326 | Common:1; Rare:77 | ||||
| chr3:45995515-45995981 | Common:3; Rare:86; Clinvar:1 |