| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:25301309-25301671 | Common:2; Rare:113 | ||||
| chr13:26221787-26221982 | Rare:57 | ||||
| chr13:27251245-27251617 | Common:6; Rare:112 | ||||
| chr13:27424509-27424740 | Common:2; Rare:76 | ||||
| chr13:27450113-27450230 | Common:3; Rare:35 | ||||
| chr13:28658904-28659194 | Rare:117; Clinvar (pathogenic):1 | ||||
| chr13:30306836-30307227 | Common:6; Rare:111 | ||||
| chr13:30307377-30307592 | Common:2; Rare:76 | ||||
| chr13:30616972-30617112 | Rare:25 | ||||
| chr13:30617233-30618039 | Common:1; Rare:244 | ||||
| chr13:32315322-32315525 | Common:1; Rare:49; Clinvar:1 | ||||
| chr13:33285683-33285944 | Common:1; Rare:57 | ||||
| chr13:33818024-33818189 | Common:1; Rare:72 | ||||
| chr13:36345513-36345663 | Common:1; Rare:32 | ||||
| chr13:36346240-36346466 | Common:2; Rare:56; Clinvar:1; Clinvar (benign):1 |