| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:23917651-23918031 | Common:2; Rare:99; Clinvar (benign):1 | ||||
| chr3:25789924-25790118 | Common:4; Rare:72 | ||||
| chr3:28348607-28348727 | Rare:27 | ||||
| chr3:28348760-28349179 | Common:3; Rare:137 | ||||
| chr3:29280852-29281102 | Common:3; Rare:49 | ||||
| chr3:29281104-29281428 | Common:12; Rare:58 | ||||
| chr3:30606269-30606521 | Common:1; Rare:59; Clinvar:1 | ||||
| chr3:31981524-31981776 | Rare:57 | ||||
| chr3:32570738-32570914 | Rare:84 | ||||
| chr3:33097090-33097286 | Common:3; Rare:66; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:33277295-33277495 | Common:2; Rare:54 | ||||
| chr3:33798514-33798672 | Common:2; Rare:56 | ||||
| chr3:36993067-36993563 | Common:2; Rare:168; Clinvar:27; Clinvar (benign):12; Clinvar (pathogenic):3 | ||||
| chr3:37176237-37176389 | Rare:50 | ||||
| chr3:37243193-37243348 | Common:1; Rare:40 |