| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:12664084-12664330 | Common:1; Rare:67; Clinvar:1; Clinvar (benign):2 | ||||
| chr3:13420226-13420458 | Common:1; Rare:66 | ||||
| chr3:13480040-13480334 | Common:2; Rare:69 | ||||
| chr3:14124703-14125173 | Common:4; Rare:139; Clinvar:4; Clinvar (benign):1 | ||||
| chr3:14178564-14178720 | Common:2; Rare:101; Clinvar:4; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr3:14178733-14178866 | Rare:53 | ||||
| chr3:14402433-14402628 | Rare:48 | ||||
| chr3:14651485-14651847 | Rare:114 | ||||
| chr3:14947196-14947563 | Common:4; Rare:160 | ||||
| chr3:14948027-14948202 | Rare:79 | ||||
| chr3:14948363-14948641 | Common:2; Rare:78 | ||||
| chr3:15427424-15427629 | Common:1; Rare:65 | ||||
| chr3:15601506-15601814 | Common:4; Rare:130; Clinvar:2 | ||||
| chr3:15859803-15860140 | Common:4; Rare:106 | ||||
| chr3:16264875-16265243 | Common:2; Rare:121 |