| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:9749839-9750104 | Common:1; Rare:79 | ||||
| chr3:9769853-9770031 | Common:1; Rare:48 | ||||
| chr3:9792369-9792611 | Rare:66 | ||||
| chr3:9792667-9793123 | Common:3; Rare:158 | ||||
| chr3:9843963-9844126 | Common:2; Rare:66 | ||||
| chr3:9890510-9890703 | Common:2; Rare:76 | ||||
| chr3:9933507-9933910 | Common:3; Rare:157; Clinvar:3 | ||||
| chr3:9986539-9987174 | Common:7; Rare:189 | ||||
| chr3:10026298-10026473 | Rare:57 | ||||
| chr3:10115515-10115768 | Common:4; Rare:87 | ||||
| chr3:10141664-10141862 | Common:1; Rare:90; Clinvar:13; Clinvar (benign):17 | ||||
| chr3:10142141-10142172 | Rare:13; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr3:10321048-10321240 | Common:2; Rare:88 | ||||
| chr3:10707966-10708221 | Rare:66 | ||||
| chr3:11154338-11154502 | Common:4; Rare:46 |