| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:42804407-42804663 | Common:2; Rare:76 | ||||
| chr3:43690769-43690942 | Common:1; Rare:76; Clinvar:5; Clinvar (benign):1 | ||||
| chr3:44338706-44338800 | Common:3; Rare:33 | ||||
| chr3:44477655-44477807 | Common:1; Rare:28 | ||||
| chr3:44624850-44625063 | Common:2; Rare:59 | ||||
| chr3:44712604-44712720 | Common:1; Rare:53 | ||||
| chr3:44729549-44729687 | Common:1; Rare:52 | ||||
| chr3:44761577-44761794 | Common:3; Rare:83 | ||||
| chr3:44861767-44861926 | Common:2; Rare:71 | ||||
| chr3:44976051-44976268 | Common:3; Rare:85 | ||||
| chr3:45026060-45026333 | Common:3; Rare:49 | ||||
| chr3:45388386-45388611 | Common:1; Rare:62 | ||||
| chr3:45689186-45689461 | Common:1; Rare:94 | ||||
| chr3:45842054-45842287 | Common:1; Rare:61 | ||||
| chr3:45995809-45995970 | Common:2; Rare:36; Clinvar:1 |