| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:45206401-45206645 | Common:1; Rare:34 | ||||
| chr13:45341036-45341617 | Common:4; Rare:260 | ||||
| chr13:45418330-45418541 | Rare:64 | ||||
| chr13:45464713-45465026 | Common:1; Rare:77 | ||||
| chr13:46052627-46052821 | Common:2; Rare:49 | ||||
| chr13:46182102-46182446 | Common:3; Rare:59 | ||||
| chr13:46211801-46212013 | Common:2; Rare:66 | ||||
| chr13:46387193-46387367 | Rare:46 | ||||
| chr13:46387452-46387511 | Rare:12 | ||||
| chr13:46553014-46553316 | Common:2; Rare:97 | ||||
| chr13:46797103-46797262 | Common:2; Rare:53 | ||||
| chr13:48001242-48001389 | Common:1; Rare:70; Clinvar:3; Clinvar (benign):4 | ||||
| chr13:48037410-48037795 | Common:2; Rare:155 | ||||
| chr13:48037932-48038069 | Common:4; Rare:41 | ||||
| chr13:48233060-48233475 | Common:3; Rare:144 |