| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:28718555-28718759 | Common:3; Rare:40 | ||||
| chr13:28718764-28719123 | Common:1; Rare:94 | ||||
| chr13:29849829-29850225 | Common:1; Rare:114 | ||||
| chr13:29850286-29850429 | Common:2; Rare:45 | ||||
| chr13:30306840-30307203 | Common:6; Rare:97 | ||||
| chr13:30307386-30307597 | Common:2; Rare:72 | ||||
| chr13:30617519-30618046 | Common:1; Rare:170 | ||||
| chr13:32031398-32031648 | Rare:51 | ||||
| chr13:32315435-32315531 | Rare:27; Clinvar:1 | ||||
| chr13:32428084-32428418 | Rare:68 | ||||
| chr13:32586234-32586555 | Common:1; Rare:95 | ||||
| chr13:33285662-33285887 | Rare:52 | ||||
| chr13:34942181-34942298 | Common:2; Rare:36 | ||||
| chr13:35476687-35476809 | Common:1; Rare:17 | ||||
| chr13:36346260-36346457 | Common:2; Rare:52; Clinvar:1; Clinvar (benign):1 |