| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:131381445-131381901 | Common:4; Rare:135 | ||||
| chr3:131502765-131503025 | Common:1; Rare:103 | ||||
| chr3:132417171-132417544 | Common:5; Rare:122 | ||||
| chr3:132659726-132659970 | Common:3; Rare:60 | ||||
| chr3:132660945-132661126 | Common:1; Rare:44 | ||||
| chr3:132661217-132661296 | Rare:10 | ||||
| chr3:132722002-132722305 | Common:2; Rare:114; Clinvar:22; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
| chr3:133573796-133574025 | Rare:80 | ||||
| chr3:133661856-133662040 | Rare:44 | ||||
| chr3:134029707-134030028 | Common:4; Rare:90 | ||||
| chr3:134374400-134374634 | Common:1; Rare:65 | ||||
| chr3:134485488-134485760 | Rare:66 | ||||
| chr3:134485957-134486229 | Common:2; Rare:93 | ||||
| chr3:135965900-135966043 | Rare:49 | ||||
| chr3:136752341-136752521 | Common:1; Rare:44 |