| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:48685603-48685713 | Rare:23 | ||||
| chr3:48685766-48686034 | Common:2; Rare:87 | ||||
| chr3:48716394-48716715 | Rare:63 | ||||
| chr3:48717142-48717487 | Common:3; Rare:76 | ||||
| chr3:48847564-48848026 | Common:1; Rare:122 | ||||
| chr3:48898796-48899063 | Rare:81; Clinvar:7; Clinvar (benign):1 | ||||
| chr3:48918304-48918549 | Rare:80 | ||||
| chr3:48918597-48919162 | Common:3; Rare:240 | ||||
| chr3:48919801-48920029 | Common:1; Rare:38 | ||||
| chr3:48989727-48989979 | Rare:59 | ||||
| chr3:48990112-48990315 | Rare:42 | ||||
| chr3:48990336-48990487 | Rare:55 | ||||
| chr3:48990890-48991060 | Rare:28 | ||||
| chr3:49007090-49007480 | Common:2; Rare:148 | ||||
| chr3:49007796-49008073 | Common:2; Rare:80 |