| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:37577585-37577816 | Rare:50 | ||||
| chr13:37596939-37597009 | Common:2; Rare:9 | ||||
| chr13:40921659-40921914 | Common:5; Rare:69 | ||||
| chr13:48413059-48413172 | Rare:16 | ||||
| chr13:52617325-52617537 | Rare:51 | ||||
| chr13:57629915-57630115 | Common:1; Rare:56 | ||||
| chr13:87671164-87671392 | Common:1; Rare:65 | ||||
| chr13:93227487-93227609 | Rare:51; Clinvar:1 | ||||
| chr13:97432974-97433085 | Common:2; Rare:36 | ||||
| chr13:99087946-99088171 | Common:2; Rare:51 | ||||
| chr13:110174444-110174742 | Rare:98; Clinvar (benign):3 | ||||
| chr13:110177840-110178235 | Rare:107; Clinvar:3; Clinvar (benign):4 | ||||
| chr13:110178921-110179352 | Common:4; Rare:116; Clinvar:2; Clinvar (benign):1 | ||||
| chr13:110205351-110205539 | Common:1; Rare:74; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr13:110212415-110212574 | Common:1; Rare:51; Clinvar (benign):1 |