| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:45842041-45842305 | Common:1; Rare:72 | ||||
| chr3:45995814-45995975 | Common:2; Rare:36; Clinvar:1 | ||||
| chr3:46979504-46979857 | Common:3; Rare:91; Clinvar:2 | ||||
| chr3:47163869-47164250 | Common:1; Rare:106; Clinvar (pathogenic):1 | ||||
| chr3:47380780-47381073 | Rare:94 | ||||
| chr3:47381427-47381524 | Rare:26 | ||||
| chr3:47475812-47476114 | Common:5; Rare:120 | ||||
| chr3:47513306-47513517 | Common:1; Rare:57 | ||||
| chr3:47513655-47513788 | Rare:41 | ||||
| chr3:47781668-47782025 | Rare:130 | ||||
| chr3:47802885-47803203 | Common:1; Rare:94 | ||||
| chr3:47803423-47803592 | Common:2; Rare:42 | ||||
| chr3:48088785-48089092 | Rare:105 | ||||
| chr3:48188446-48188728 | Common:2; Rare:68 | ||||
| chr3:48240985-48241203 | Common:3; Rare:74 |