| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:50252214-50252538 | Common:1; Rare:68 | ||||
| chr3:52517364-52517586 | Rare:79 | ||||
| chr3:53233230-53233549 | Common:3; Rare:91; Clinvar (pathogenic):1 | ||||
| chr3:54888962-54889143 | Common:1; Rare:29 | ||||
| chr3:57892539-57892635 | Rare:16 | ||||
| chr3:57952311-57952549 | Rare:39 | ||||
| chr3:61560867-61561058 | Common:3; Rare:57 | ||||
| chr3:61743134-61743403 | Common:3; Rare:53 | ||||
| chr3:62150062-62150255 | Rare:44 | ||||
| chr3:64010241-64010260 | Rare:8 | ||||
| chr3:64561078-64561528 | Common:6; Rare:83 | ||||
| chr3:64685062-64685307 | Rare:59 | ||||
| chr3:71064172-71064189 | Rare:6 | ||||
| chr3:71100433-71100576 | Rare:27 | ||||
| chr3:73405928-73406154 | Common:2; Rare:45 |