| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:37527850-37528175 | Common:4; Rare:108 | ||||
| chr20:38033415-38033757 | Common:2; Rare:100 | ||||
| chr20:38165265-38165373 | Rare:34 | ||||
| chr20:38962150-38962382 | Common:1; Rare:96 | ||||
| chr20:43458025-43458422 | Common:3; Rare:166 | ||||
| chr20:43590664-43590990 | Rare:66 | ||||
| chr20:44210702-44211105 | Common:5; Rare:145 | ||||
| chr20:44582464-44582667 | Rare:30 | ||||
| chr20:44651678-44651858 | Common:1; Rare:46; Clinvar (benign):1 | ||||
| chr20:44966370-44966543 | Rare:69 | ||||
| chr20:45348404-45348540 | Common:1; Rare:33 | ||||
| chr20:45791884-45792014 | Common:1; Rare:51 | ||||
| chr20:45857343-45857602 | Common:3; Rare:67 | ||||
| chr20:45891206-45891413 | Common:1; Rare:64; Clinvar:3; Clinvar (benign):1 | ||||
| chr20:45934670-45934703 | Rare:14 |