| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:46211786-46212030 | Common:2; Rare:73 | ||||
| chr13:46387197-46387351 | Rare:38 | ||||
| chr13:46553056-46553310 | Common:2; Rare:74 | ||||
| chr13:48001231-48001408 | Common:1; Rare:81; Clinvar:3; Clinvar (benign):6 | ||||
| chr13:48037634-48037789 | Common:1; Rare:72 | ||||
| chr13:48233060-48233475 | Common:3; Rare:144 | ||||
| chr13:48303664-48303900 | Rare:80; Clinvar:3; Clinvar (pathogenic):1 | ||||
| chr13:48533038-48533111 | Common:2; Rare:23 | ||||
| chr13:48975819-48975961 | Rare:50 | ||||
| chr13:48976362-48976824 | Common:3; Rare:143 | ||||
| chr13:49247830-49247990 | Rare:50 | ||||
| chr13:49444005-49444476 | Common:1; Rare:152 | ||||
| chr13:49628356-49628563 | Common:1; Rare:49 | ||||
| chr13:49936260-49936585 | Common:1; Rare:96 | ||||
| chr13:49996748-49997092 | Common:1; Rare:70 |