| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:41060873-41061249 | Common:17; Rare:173 | ||||
| chr13:41061364-41061635 | Common:2; Rare:84 | ||||
| chr13:41132759-41132938 | Rare:41 | ||||
| chr13:41457247-41457547 | Common:2; Rare:79 | ||||
| chr13:43879464-43879614 | Rare:41 | ||||
| chr13:43879684-43879910 | Common:18; Rare:64 | ||||
| chr13:44435155-44435447 | Common:3; Rare:86 | ||||
| chr13:44989449-44989628 | Rare:67 | ||||
| chr13:45120392-45120570 | Common:1; Rare:58 | ||||
| chr13:45341040-45341609 | Common:4; Rare:258 | ||||
| chr13:46052696-46052867 | Common:2; Rare:48 | ||||
| chr13:46182131-46182450 | Common:3; Rare:52 | ||||
| chr13:48001253-48001410 | Common:1; Rare:72; Clinvar:3; Clinvar (benign):3 | ||||
| chr13:48037636-48037789 | Common:1; Rare:71 | ||||
| chr13:48233046-48233363 | Common:3; Rare:108 |