| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:43023476-43023732 | Common:2; Rare:98 | ||||
| chr13:43879440-43879967 | Common:19; Rare:134 | ||||
| chr13:43880028-43880063 | Rare:5 | ||||
| chr13:44436783-44436987 | Common:2; Rare:59 | ||||
| chr13:44989428-44989616 | Rare:71 | ||||
| chr13:45120392-45120612 | Common:1; Rare:72 | ||||
| chr13:45341036-45341609 | Common:4; Rare:259 | ||||
| chr13:45464695-45465018 | Common:1; Rare:77 | ||||
| chr13:46052671-46052842 | Common:2; Rare:46 | ||||
| chr13:46797098-46797349 | Common:3; Rare:85 | ||||
| chr13:48037645-48037801 | Common:1; Rare:79; Clinvar:1 | ||||
| chr13:48233087-48233369 | Rare:93 | ||||
| chr13:48303667-48303763 | Rare:38; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr13:48975628-48975932 | Common:2; Rare:94 | ||||
| chr13:48976533-48976837 | Common:1; Rare:88 |