| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:25863250-25863421 | Common:2; Rare:66 | ||||
| chr20:25868151-25868311 | Common:1; Rare:43 | ||||
| chr20:31514323-31514524 | Common:6; Rare:93 | ||||
| chr20:31547294-31547438 | Rare:36 | ||||
| chr20:31722776-31722964 | Rare:47 | ||||
| chr20:31723505-31723713 | Common:1; Rare:59 | ||||
| chr20:31739086-31739364 | Common:2; Rare:73 | ||||
| chr20:32109421-32109780 | Common:2; Rare:103 | ||||
| chr20:32207703-32207939 | Common:3; Rare:91 | ||||
| chr20:32483366-32483798 | Common:1; Rare:69 | ||||
| chr20:33401476-33401593 | Rare:33 | ||||
| chr20:33720210-33720500 | Common:4; Rare:73 | ||||
| chr20:33993814-33994120 | Common:1; Rare:116 | ||||
| chr20:34112195-34112423 | Rare:65 | ||||
| chr20:34302968-34303295 | Rare:103; Clinvar (benign):1 |