| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:36346632-36346783 | Common:4; Rare:44 | ||||
| chr13:37000761-37000815 | Rare:28; Clinvar (pathogenic):1 | ||||
| chr13:37059600-37059751 | Common:1; Rare:51 | ||||
| chr13:38350217-38350376 | Rare:52 | ||||
| chr13:39037572-39037871 | Common:1; Rare:97 | ||||
| chr13:39038064-39038629 | Common:1; Rare:148 | ||||
| chr13:39655618-39655769 | Common:2; Rare:82; Clinvar:3; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr13:40789377-40789621 | Common:2; Rare:81; Clinvar:5; Clinvar (benign):2 | ||||
| chr13:41060153-41060541 | Common:3; Rare:137 | ||||
| chr13:41060846-41061649 | Common:20; Rare:328 | ||||
| chr13:41132731-41132984 | Rare:71 | ||||
| chr13:42040294-42040595 | Common:2; Rare:93 | ||||
| chr13:42271794-42272046 | Common:2; Rare:72 | ||||
| chr13:42992133-42992321 | Common:2; Rare:44 | ||||
| chr13:43023470-43023727 | Common:1; Rare:98 |