| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:35664862-35665029 | Common:1; Rare:45 | ||||
| chr20:35699336-35699460 | Rare:38 | ||||
| chr20:35740804-35741147 | Common:3; Rare:97 | ||||
| chr20:35742175-35742651 | Common:5; Rare:153 | ||||
| chr20:35771754-35772055 | Common:2; Rare:89 | ||||
| chr20:36541366-36541572 | Common:2; Rare:59 | ||||
| chr20:36951599-36951981 | Common:1; Rare:124; Clinvar:2; Clinvar (benign):4 | ||||
| chr20:37178871-37179165 | Rare:84 | ||||
| chr20:37179519-37179612 | Common:1; Rare:37 | ||||
| chr20:38033416-38033791 | Common:2; Rare:109 | ||||
| chr20:38165188-38165403 | Common:1; Rare:74 | ||||
| chr20:38259972-38260282 | Rare:48 | ||||
| chr20:38805584-38805718 | Common:2; Rare:33 | ||||
| chr20:38962154-38962388 | Common:1; Rare:98 | ||||
| chr20:41352652-41352823 | Rare:46 |