| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:59391739-59391907 | Rare:43 | ||||
| chr13:59409734-59410065 | Rare:65 | ||||
| chr13:59458967-59459175 | Common:1; Rare:37 | ||||
| chr13:59531591-59531855 | Rare:57 | ||||
| chr13:59542441-59542730 | Common:1; Rare:48 | ||||
| chr13:59545144-59545359 | Common:1; Rare:38 | ||||
| chr13:59565612-59565821 | Common:1; Rare:46 | ||||
| chr13:59665876-59666018 | Rare:24 | ||||
| chr13:59666614-59666825 | Common:1; Rare:77; Clinvar:1; Clinvar (benign):1 | ||||
| chr13:59667084-59667093 | Rare:1 | ||||
| chr13:59671852-59672181 | Common:1; Rare:66 | ||||
| chr13:59673575-59673679 | Rare:14 | ||||
| chr13:59679410-59679470 | Rare:13 | ||||
| chr13:59681757-59681894 | Rare:23 | ||||
| chr13:59683971-59684233 | Rare:59 |