| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:44648829-44649229 | Common:1; Rare:85 | ||||
| chr3:44712426-44712826 | Common:4; Rare:243 | ||||
| chr3:44729370-44729770 | Common:16; Rare:487 | ||||
| chr3:44761474-44761874 | Common:21; Rare:774 | ||||
| chr3:44761929-44762220 | Rare:63 | ||||
| chr3:44762261-44762704 | Common:2; Rare:121 | ||||
| chr3:44975219-44975720 | Common:4; Rare:150 | ||||
| chr3:44975995-44976395 | Common:23; Rare:691 | ||||
| chr3:45138961-45139907 | Common:22; Rare:330 | ||||
| chr3:45145620-45146116 | Common:11; Rare:161 | ||||
| chr3:45146236-45146636 | Common:6; Rare:356 | ||||
| chr3:45226220-45226560 | Rare:340 | ||||
| chr3:45388305-45388787 | Common:15; Rare:488; Clinvar (benign):1 | ||||
| chr3:45593747-45593953 | Common:10; Rare:92 | ||||
| chr3:45593960-45594731 | Common:18; Rare:601 |