| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:25696800-25697062 | Common:3; Rare:76 | ||||
| chr20:31547305-31547438 | Rare:34 | ||||
| chr20:31605680-31605742 | Common:1; Rare:30 | ||||
| chr20:31637763-31637938 | Rare:46; Clinvar:1 | ||||
| chr20:31722514-31722644 | Rare:21 | ||||
| chr20:31723519-31723791 | Common:2; Rare:88 | ||||
| chr20:31739085-31739357 | Common:2; Rare:69 | ||||
| chr20:32207712-32207944 | Common:3; Rare:91 | ||||
| chr20:32483440-32483752 | Common:1; Rare:51 | ||||
| chr20:33401476-33401612 | Rare:35 | ||||
| chr20:33720205-33720540 | Common:4; Rare:87 | ||||
| chr20:33731987-33732012 | Rare:13 | ||||
| chr20:34112102-34112412 | Rare:100 | ||||
| chr20:34303283-34303357 | Common:1; Rare:51; Clinvar:2; Clinvar (benign):1 | ||||
| chr20:34677086-34677291 | Rare:54 |