| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:48095033-48095265 | Common:4; Rare:260 | ||||
| chr13:48232972-48233403 | Common:6; Rare:312 | ||||
| chr13:48233376-48233715 | Common:4; Rare:104 | ||||
| chr13:48253551-48253924 | Common:4; Rare:142 | ||||
| chr13:48303600-48304038 | Common:1; Rare:321; Clinvar:23; Clinvar (benign):8; Clinvar (pathogenic):4 | ||||
| chr13:48532560-48532960 | Common:13; Rare:330 | ||||
| chr13:48975237-48975976 | Common:3; Rare:244 | ||||
| chr13:48976121-48976307 | Rare:83 | ||||
| chr13:48976354-48976880 | Common:7; Rare:384 | ||||
| chr13:49110080-49110389 | Common:5; Rare:141 | ||||
| chr13:49219950-49220400 | Common:3; Rare:178 | ||||
| chr13:49247788-49248008 | Rare:164 | ||||
| chr13:49401350-49401840 | Common:2; Rare:121 | ||||
| chr13:49443897-49444549 | Common:6; Rare:493 | ||||
| chr13:49495856-49496088 | Rare:109 |