| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:4814416-4814817 | Common:7; Rare:110; Clinvar:1; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr3:4979224-4979542 | Common:2; Rare:74 | ||||
| chr3:5187312-5187663 | Common:5; Rare:136 | ||||
| chr3:8501633-8501931 | Common:2; Rare:109 | ||||
| chr3:9362936-9363214 | Common:4; Rare:84 | ||||
| chr3:9397430-9397891 | Common:1; Rare:148 | ||||
| chr3:9749841-9750362 | Common:2; Rare:166 | ||||
| chr3:9769892-9770057 | Common:1; Rare:43 | ||||
| chr3:9792375-9792586 | Rare:59 | ||||
| chr3:9792676-9793124 | Common:3; Rare:157 | ||||
| chr3:9843968-9844141 | Common:2; Rare:69 | ||||
| chr3:9890294-9890703 | Common:4; Rare:140 | ||||
| chr3:9916892-9917154 | Common:3; Rare:61 | ||||
| chr3:9933507-9933868 | Common:2; Rare:146; Clinvar:3 | ||||
| chr3:9986635-9987174 | Common:5; Rare:159 |