| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:58433769-58433773 | Rare:2 | ||||
| chr3:58491793-58492143 | Common:3; Rare:87 | ||||
| chr3:61251383-61251593 | Common:4; Rare:53 | ||||
| chr3:62318932-62319055 | Rare:48 | ||||
| chr3:63863771-63864132 | Common:7; Rare:120 | ||||
| chr3:67654570-67654727 | Common:1; Rare:61 | ||||
| chr3:69013249-69013333 | Rare:25 | ||||
| chr3:69084758-69085054 | Common:3; Rare:74 | ||||
| chr3:81761592-81761989 | Common:3; Rare:115; Clinvar:1 | ||||
| chr3:87227062-87227366 | Common:1; Rare:96; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:88058923-88059294 | Common:3; Rare:137 | ||||
| chr3:88149819-88150009 | Rare:53 | ||||
| chr3:93980074-93980195 | Common:4; Rare:54; Clinvar:1; Clinvar (benign):2 | ||||
| chr3:94062910-94063083 | Rare:40 | ||||
| chr3:97764448-97764795 | Common:1; Rare:81; Clinvar (benign):1 |