| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:50582801-50583120 | Common:6; Rare:92; Clinvar:2; Clinvar (benign):2 | ||||
| chr22:50783601-50783853 | Common:2; Rare:78 | ||||
| chr3:3126793-3126984 | Common:4; Rare:79; Clinvar (benign):1 | ||||
| chr3:3800887-3801043 | Common:1; Rare:46 | ||||
| chr3:4467246-4467334 | Rare:35; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:8501571-8501937 | Common:3; Rare:141 | ||||
| chr3:9362984-9363117 | Common:1; Rare:52 | ||||
| chr3:9397437-9397670 | Rare:77 | ||||
| chr3:9749690-9749983 | Rare:92 | ||||
| chr3:9792374-9792524 | Rare:44 | ||||
| chr3:9792705-9793124 | Common:3; Rare:148 | ||||
| chr3:9843968-9844163 | Common:2; Rare:73 | ||||
| chr3:9933544-9933857 | Common:2; Rare:125; Clinvar:2 | ||||
| chr3:10026295-10026492 | Rare:63 | ||||
| chr3:10115520-10115730 | Common:3; Rare:77 |