| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:25783371-25783634 | Common:2; Rare:90; Clinvar (benign):3 | ||||
| chr3:25790007-25790124 | Common:3; Rare:46 | ||||
| chr3:27484136-27484311 | Common:2; Rare:60 | ||||
| chr3:27722317-27722435 | Rare:35 | ||||
| chr3:28291732-28291860 | Common:1; Rare:25 | ||||
| chr3:28348592-28348741 | Rare:32 | ||||
| chr3:28348771-28349218 | Common:4; Rare:147 | ||||
| chr3:29280837-29281102 | Common:3; Rare:55 | ||||
| chr3:30606339-30606948 | Common:2; Rare:175; Clinvar:9; Clinvar (benign):4 | ||||
| chr3:31532375-31532733 | Common:4; Rare:110 | ||||
| chr3:31532850-31533224 | Common:2; Rare:149; Clinvar (benign):2 | ||||
| chr3:31981613-31981820 | Common:1; Rare:54 | ||||
| chr3:32106418-32106714 | Common:4; Rare:82; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:32502770-32502910 | Rare:45 | ||||
| chr3:32570636-32570998 | Common:1; Rare:158 |