| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:44510535-44510725 | Common:8; Rare:124 | ||||
| chr3:44624814-44625123 | Common:5; Rare:142 | ||||
| chr3:44648639-44648824 | Rare:43 | ||||
| chr3:44761585-44761916 | Common:9; Rare:316 | ||||
| chr3:44761969-44762171 | Rare:35 | ||||
| chr3:44861704-44861973 | Common:8; Rare:270 | ||||
| chr3:44862080-44862310 | Common:12; Rare:178 | ||||
| chr3:44974595-44975392 | Common:7; Rare:208 | ||||
| chr3:44976041-44976352 | Common:10; Rare:320 | ||||
| chr3:45226244-45226500 | Rare:89 | ||||
| chr3:45388376-45388736 | Common:5; Rare:169; Clinvar (benign):1 | ||||
| chr3:45593703-45594318 | Common:20; Rare:437 | ||||
| chr3:45689008-45689509 | Common:7; Rare:447 | ||||
| chr3:45842043-45842342 | Common:3; Rare:218 | ||||
| chr3:45995523-45995894 | Rare:141; Clinvar:3 |