| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:30307372-30307605 | Common:3; Rare:78 | ||||
| chr13:30465797-30466117 | Common:1; Rare:102 | ||||
| chr13:30617530-30618011 | Common:1; Rare:156 | ||||
| chr13:32315342-32315553 | Common:1; Rare:61; Clinvar:2; Clinvar (benign):2 | ||||
| chr13:33285710-33285936 | Common:1; Rare:51 | ||||
| chr13:36346287-36346454 | Common:2; Rare:44; Clinvar:1; Clinvar (benign):1 | ||||
| chr13:36999266-36999465 | Rare:80 | ||||
| chr13:37000750-37000808 | Rare:26 | ||||
| chr13:37059621-37059726 | Common:1; Rare:34 | ||||
| chr13:41060880-41061654 | Common:20; Rare:307 | ||||
| chr13:43023508-43023720 | Common:1; Rare:87 | ||||
| chr13:43879492-43879648 | Common:1; Rare:41 | ||||
| chr13:43879710-43879910 | Common:18; Rare:59 | ||||
| chr13:44989456-44989634 | Rare:66 | ||||
| chr13:45120396-45120668 | Common:1; Rare:91 |