| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:218277631-218277729 | Rare:20 | ||||
| chr2:240456685-240456825 | Rare:35 | ||||
| chr2:241064088-241064158 | Common:1; Rare:23 | ||||
| chr2:241570013-241570195 | Rare:68 | ||||
| chr2:241868171-241868336 | Common:2; Rare:31 | ||||
| chr20:2207081-2207336 | Common:2; Rare:56 | ||||
| chr20:2299632-2300046 | Common:7; Rare:90 | ||||
| chr20:2326675-2326930 | Common:4; Rare:56 | ||||
| chr20:2336027-2336219 | Common:1; Rare:47 | ||||
| chr20:3203347-3203662 | Common:2; Rare:79 | ||||
| chr20:3240177-3240258 | Rare:12 | ||||
| chr20:4822546-4822776 | Common:2; Rare:49 | ||||
| chr20:10643613-10643807 | Common:2; Rare:44; Clinvar:2; Clinvar (benign):2 | ||||
| chr20:10672523-10672707 | Common:1; Rare:48 | ||||
| chr20:10746977-10747160 | Rare:35 |