| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:31739101-31739357 | Common:1; Rare:64 | ||||
| chr20:32207703-32207939 | Common:3; Rare:91 | ||||
| chr20:32483465-32483670 | Rare:40 | ||||
| chr20:33401441-33401589 | Rare:42 | ||||
| chr20:34112102-34112423 | Rare:104 | ||||
| chr20:34303274-34303319 | Common:1; Rare:29; Clinvar (benign):1 | ||||
| chr20:34677086-34677318 | Rare:59 | ||||
| chr20:34872821-34872938 | Rare:41 | ||||
| chr20:34955755-34955868 | Common:1; Rare:41; Clinvar:2; Clinvar (benign):1 | ||||
| chr20:35147311-35147423 | Rare:31 | ||||
| chr20:35172043-35172137 | Rare:24 | ||||
| chr20:35284552-35285045 | Common:3; Rare:114 | ||||
| chr20:35557022-35557242 | Rare:69 | ||||
| chr20:35664867-35665003 | Common:1; Rare:38 | ||||
| chr20:35699312-35699460 | Rare:51; Clinvar (benign):2 |