| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:46387789-46387873 | Rare:11 | ||||
| chr13:46390164-46390378 | Common:3; Rare:32 | ||||
| chr13:46552952-46553324 | Common:2; Rare:118 | ||||
| chr13:46553734-46553792 | Rare:19 | ||||
| chr13:46679328-46679750 | Common:2; Rare:89 | ||||
| chr13:46796541-46796788 | Common:1; Rare:69 | ||||
| chr13:46796967-46797418 | Common:3; Rare:134 | ||||
| chr13:48001206-48001421 | Common:1; Rare:97; Clinvar:4; Clinvar (benign):7 | ||||
| chr13:48037320-48037848 | Common:5; Rare:192; Clinvar:2 | ||||
| chr13:48037884-48038188 | Common:5; Rare:100 | ||||
| chr13:48094397-48094692 | Common:5; Rare:69 | ||||
| chr13:48095011-48095293 | Common:2; Rare:138 | ||||
| chr13:48232981-48233445 | Common:4; Rare:149 | ||||
| chr13:48233589-48233670 | Common:1; Rare:18 | ||||
| chr13:48303212-48303943 | Rare:186; Clinvar:5; Clinvar (benign):1; Clinvar (pathogenic):1 |