| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:28393635-28393826 | Rare:50 | ||||
| chr2:28396508-28396617 | Rare:21 | ||||
| chr2:28612299-28612498 | Common:1; Rare:45 | ||||
| chr2:33225506-33225595 | Common:1; Rare:14 | ||||
| chr2:33290110-33290351 | Common:2; Rare:56 | ||||
| chr2:33316005-33316268 | Common:4; Rare:46 | ||||
| chr2:36544237-36544496 | Common:1; Rare:75 | ||||
| chr2:36548304-36548768 | Common:1; Rare:163 | ||||
| chr2:37222498-37222654 | Rare:54 | ||||
| chr2:47798417-47798678 | Common:3; Rare:94; Clinvar:20; Clinvar (benign):14; Clinvar (pathogenic):2 | ||||
| chr2:47906488-47906815 | Common:2; Rare:114 | ||||
| chr2:55282241-55282362 | Common:5; Rare:40 | ||||
| chr2:55528694-55528992 | Rare:75 | ||||
| chr2:55923051-55923157 | Rare:19 | ||||
| chr2:65018431-65018615 | Rare:45 |