| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:32315710-32316040 | Common:6; Rare:144; Clinvar (benign):8 | ||||
| chr13:32538640-32538977 | Common:2; Rare:149 | ||||
| chr13:32586248-32586616 | Common:2; Rare:111 | ||||
| chr13:33285530-33286020 | Common:2; Rare:171 | ||||
| chr13:33818007-33818231 | Common:2; Rare:181 | ||||
| chr13:36297749-36298040 | Common:4; Rare:171 | ||||
| chr13:36345840-36346263 | Common:3; Rare:120; Clinvar (benign):1 | ||||
| chr13:36346294-36347150 | Common:12; Rare:334; Clinvar:3; Clinvar (benign):3 | ||||
| chr13:36819068-36819296 | Common:1; Rare:169; Clinvar:6 | ||||
| chr13:36819300-36820110 | Common:4; Rare:278; Clinvar:15; Clinvar (benign):7; Clinvar (pathogenic):3 | ||||
| chr13:36999290-36999471 | Rare:136 | ||||
| chr13:37000225-37000415 | Common:4; Rare:65 | ||||
| chr13:37000515-37000850 | Common:6; Rare:223; Clinvar (pathogenic):2 | ||||
| chr13:37001120-37001530 | Common:4; Rare:112 | ||||
| chr13:37059569-37059775 | Common:2; Rare:111 |