| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:45003537-45003560 | Rare:5 | ||||
| chr3:45476592-45476730 | Rare:41; Clinvar (benign):1 | ||||
| chr3:45530529-45530548 | Rare:3 | ||||
| chr3:45593094-45593373 | Common:2; Rare:63 | ||||
| chr3:45643506-45643717 | Rare:49 | ||||
| chr3:45644938-45645151 | Common:1; Rare:28 | ||||
| chr3:45830912-45831126 | Rare:41 | ||||
| chr3:46989612-46989801 | Common:2; Rare:33 | ||||
| chr3:46990052-46990324 | Rare:36 | ||||
| chr3:47157461-47157593 | Rare:36 | ||||
| chr3:47164775-47164837 | Common:2; Rare:16 | ||||
| chr3:47182496-47182695 | Common:2; Rare:32 | ||||
| chr3:47340376-47340627 | Common:1; Rare:57 | ||||
| chr3:47380322-47380458 | Rare:27 | ||||
| chr3:47407132-47407363 | Common:1; Rare:64 |