| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:42633457-42633616 | Rare:40 | ||||
| chr3:42773223-42773334 | Common:1; Rare:30 | ||||
| chr3:42804427-42804663 | Common:2; Rare:71 | ||||
| chr3:43286232-43286619 | Common:1; Rare:128 | ||||
| chr3:43690622-43690989 | Common:5; Rare:153; Clinvar:7; Clinvar (benign):2 | ||||
| chr3:44624851-44625033 | Common:1; Rare:46 | ||||
| chr3:44648544-44648801 | Rare:55 | ||||
| chr3:44761590-44761809 | Common:3; Rare:79 | ||||
| chr3:44861811-44861927 | Common:2; Rare:56 | ||||
| chr3:44976120-44976295 | Common:3; Rare:75 | ||||
| chr3:45689180-45689461 | Common:1; Rare:94 | ||||
| chr3:45995800-45995882 | Rare:24; Clinvar:1 | ||||
| chr3:46693649-46693817 | Common:1; Rare:39 | ||||
| chr3:46979509-46979846 | Common:2; Rare:81; Clinvar:1 | ||||
| chr3:46981981-46982045 | Rare:10 |