| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:25664772-25665093 | Common:9; Rare:214 | ||||
| chr3:25782776-25783021 | Common:1; Rare:47 | ||||
| chr3:25783318-25783662 | Common:4; Rare:234; Clinvar:2; Clinvar (benign):6 | ||||
| chr3:25789883-25790160 | Common:12; Rare:215 | ||||
| chr3:27484146-27484878 | Common:17; Rare:520 | ||||
| chr3:27721610-27722090 | Common:6; Rare:237; Clinvar:4; Clinvar (benign):4 | ||||
| chr3:27722203-27722478 | Rare:149 | ||||
| chr3:28241357-28241809 | Common:5; Rare:348 | ||||
| chr3:28348470-28348883 | Common:3; Rare:230 | ||||
| chr3:28348874-28349246 | Common:8; Rare:298 | ||||
| chr3:30606291-30606770 | Common:3; Rare:221; Clinvar:8; Clinvar (benign):3 | ||||
| chr3:30606950-30607650 | Common:2; Rare:156; Clinvar (benign):3 | ||||
| chr3:30893989-30894852 | Common:8; Rare:330 | ||||
| chr3:31531906-31532741 | Common:29; Rare:664 | ||||
| chr3:31532764-31533101 | Common:7; Rare:322; Clinvar (benign):1 |