| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:37000736-37000815 | Rare:33; Clinvar (pathogenic):1 | ||||
| chr13:37059607-37059737 | Common:1; Rare:43 | ||||
| chr13:37869765-37869920 | Common:1; Rare:35 | ||||
| chr13:38350249-38350486 | Common:1; Rare:66 | ||||
| chr13:38686906-38687087 | Common:3; Rare:44; Clinvar:1; Clinvar (benign):1 | ||||
| chr13:39037992-39038426 | Common:1; Rare:115 | ||||
| chr13:40771128-40771289 | Common:1; Rare:53 | ||||
| chr13:40982868-40983030 | Common:3; Rare:26 | ||||
| chr13:41060428-41060511 | Rare:28 | ||||
| chr13:41060836-41061633 | Common:20; Rare:328 | ||||
| chr13:41132732-41132987 | Rare:70 | ||||
| chr13:41457292-41457547 | Common:2; Rare:75 | ||||
| chr13:43023537-43023633 | Common:1; Rare:38 | ||||
| chr13:43879492-43879614 | Rare:35 | ||||
| chr13:43879683-43879910 | Common:18; Rare:64 |