| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:42843692-42844055 | Common:2; Rare:49 | ||||
| chr3:43621914-43622316 | Common:2; Rare:118; Clinvar:7; Clinvar (benign):1 | ||||
| chr3:43690817-43691007 | Common:4; Rare:105; Clinvar:7; Clinvar (benign):3 | ||||
| chr3:44338297-44338546 | Common:3; Rare:86 | ||||
| chr3:44477655-44477707 | Common:1; Rare:10 | ||||
| chr3:44624842-44625090 | Common:2; Rare:70 | ||||
| chr3:44761565-44761794 | Common:3; Rare:93 | ||||
| chr3:44861802-44861926 | Common:2; Rare:58 | ||||
| chr3:44976054-44976280 | Common:2; Rare:89 | ||||
| chr3:45388454-45388643 | Common:1; Rare:51 | ||||
| chr3:45689070-45689370 | Common:2; Rare:107 | ||||
| chr3:45943339-45943469 | Rare:21 | ||||
| chr3:45995739-45995975 | Common:2; Rare:52; Clinvar:1 | ||||
| chr3:46407074-46407273 | Rare:40 | ||||
| chr3:46566182-46566512 | Rare:65 |