| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:44989432-44989621 | Rare:72 | ||||
| chr13:45120383-45120570 | Common:2; Rare:62 | ||||
| chr13:45341040-45341650 | Common:4; Rare:272 | ||||
| chr13:45418322-45418548 | Rare:70 | ||||
| chr13:46052709-46052795 | Common:1; Rare:23 | ||||
| chr13:46182151-46182450 | Common:3; Rare:50 | ||||
| chr13:46797103-46797261 | Common:2; Rare:53 | ||||
| chr13:48001246-48001397 | Common:1; Rare:71; Clinvar:3; Clinvar (benign):4 | ||||
| chr13:48037610-48037783 | Common:1; Rare:77 | ||||
| chr13:48037918-48038027 | Common:4; Rare:40 | ||||
| chr13:48233064-48233369 | Common:1; Rare:104 | ||||
| chr13:48303674-48303900 | Rare:76; Clinvar:3; Clinvar (pathogenic):1 | ||||
| chr13:48975790-48975923 | Common:1; Rare:50 | ||||
| chr13:49247807-49247982 | Rare:50 | ||||
| chr13:49443997-49444442 | Common:1; Rare:142 |