| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:100515567-100515780 | Common:4; Rare:59; Clinvar (benign):1 | ||||
| chr13:100588348-100588435 | Rare:25 | ||||
| chr13:100588708-100588863 | Common:4; Rare:50 | ||||
| chr13:100674657-100675234 | Common:7; Rare:231 | ||||
| chr13:102401088-102401408 | Rare:67 | ||||
| chr13:102402230-102402589 | Common:1; Rare:65 | ||||
| chr13:102596658-102597039 | Common:1; Rare:153 | ||||
| chr13:102773484-102773574 | Rare:21 | ||||
| chr13:102773632-102773958 | Common:1; Rare:122 | ||||
| chr13:102798510-102798542 | Rare:11 | ||||
| chr13:102798901-102799205 | Common:1; Rare:63 | ||||
| chr13:102800004-102800533 | Common:2; Rare:129 | ||||
| chr13:102845619-102845956 | Common:6; Rare:95; Clinvar (benign):3 | ||||
| chr13:102846010-102846181 | Common:3; Rare:38; Clinvar:4; Clinvar (benign):1 | ||||
| chr13:102846495-102846867 | Common:2; Rare:80 |