| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:42804415-42804657 | Common:2; Rare:71 | ||||
| chr3:43286442-43286612 | Common:1; Rare:79 | ||||
| chr3:43621914-43622322 | Common:2; Rare:119; Clinvar:7; Clinvar (benign):1 | ||||
| chr3:43690811-43690933 | Common:1; Rare:50; Clinvar:5; Clinvar (benign):1 | ||||
| chr3:44338027-44338147 | Common:2; Rare:37 | ||||
| chr3:44477625-44477746 | Common:1; Rare:27 | ||||
| chr3:44555162-44555260 | Rare:26 | ||||
| chr3:44624886-44625095 | Common:2; Rare:61 | ||||
| chr3:44648628-44648804 | Rare:44 | ||||
| chr3:44729543-44729667 | Common:1; Rare:48 | ||||
| chr3:44761577-44761867 | Common:3; Rare:110 | ||||
| chr3:44861694-44861925 | Common:3; Rare:88 | ||||
| chr3:44976074-44976301 | Common:3; Rare:93 | ||||
| chr3:45146335-45146504 | Common:1; Rare:56 | ||||
| chr3:45388436-45388616 | Rare:45 |