| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:41060854-41061669 | Common:20; Rare:331 | ||||
| chr13:41132688-41132964 | Rare:67 | ||||
| chr13:41374114-41374122 | Rare:2 | ||||
| chr13:43879452-43879646 | Rare:49 | ||||
| chr13:43879743-43879825 | Common:9; Rare:31 | ||||
| chr13:44436637-44436725 | Common:1; Rare:24 | ||||
| chr13:44576325-44576399 | Common:1; Rare:22 | ||||
| chr13:44989449-44989735 | Rare:106 | ||||
| chr13:45120392-45120553 | Common:1; Rare:52 | ||||
| chr13:45340711-45341610 | Common:7; Rare:390 | ||||
| chr13:46052671-46052841 | Common:2; Rare:45 | ||||
| chr13:46553170-46553193 | Common:1; Rare:6 | ||||
| chr13:48037654-48037769 | Rare:54 | ||||
| chr13:48303537-48303913 | Rare:112; Clinvar:3; Clinvar (pathogenic):1 | ||||
| chr13:48975852-48975952 | Rare:29 |