| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:9792705-9793124 | Common:3; Rare:148 | ||||
| chr3:9843975-9844136 | Common:2; Rare:63 | ||||
| chr3:9916829-9917207 | Common:4; Rare:77 | ||||
| chr3:9933523-9933908 | Common:3; Rare:152; Clinvar:3 | ||||
| chr3:9933992-9934065 | Rare:19 | ||||
| chr3:10026024-10026195 | Common:2; Rare:34 | ||||
| chr3:10026295-10026484 | Rare:62 | ||||
| chr3:10505511-10505811 | Common:2; Rare:59 | ||||
| chr3:11154383-11154507 | Common:3; Rare:34 | ||||
| chr3:12664075-12664330 | Common:1; Rare:70; Clinvar:1; Clinvar (benign):3 | ||||
| chr3:13420214-13420469 | Common:1; Rare:76 | ||||
| chr3:13480040-13480334 | Common:2; Rare:69 | ||||
| chr3:14124703-14125145 | Common:4; Rare:130; Clinvar:4; Clinvar (benign):1 | ||||
| chr3:14178545-14178880 | Common:2; Rare:174; Clinvar:4; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr3:14651486-14651818 | Rare:98 |