| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:77919397-77919657 | Common:1; Rare:95; Clinvar:2; Clinvar (benign):1 | ||||
| chr13:79405740-79405956 | Common:1; Rare:68 | ||||
| chr13:79406219-79406332 | Common:3; Rare:36 | ||||
| chr13:79481003-79481467 | Common:2; Rare:180 | ||||
| chr13:93227032-93227458 | Common:1; Rare:98; Clinvar:6; Clinvar (benign):1 | ||||
| chr13:94596106-94596369 | Common:2; Rare:92 | ||||
| chr13:94601646-94601924 | Common:3; Rare:77 | ||||
| chr13:95676894-95677241 | Common:4; Rare:129 | ||||
| chr13:96053344-96053519 | Common:2; Rare:80 | ||||
| chr13:99200668-99200894 | Common:6; Rare:104 | ||||
| chr13:99606507-99606698 | Common:5; Rare:55 | ||||
| chr13:100088843-100089133 | Rare:114; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr13:100674761-100675055 | Common:3; Rare:117 | ||||
| chr13:102596736-102597074 | Common:1; Rare:141; Clinvar (benign):1 | ||||
| chr13:106567919-106568283 | Rare:98 |