| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:48001262-48001380 | Common:1; Rare:55; Clinvar:3; Clinvar (benign):2 | ||||
| chr13:48037610-48037771 | Rare:68 | ||||
| chr13:48037912-48038141 | Common:5; Rare:70 | ||||
| chr13:48303674-48303900 | Rare:76; Clinvar:3; Clinvar (pathogenic):1 | ||||
| chr13:48533069-48533171 | Common:1; Rare:31 | ||||
| chr13:48975830-48975950 | Rare:45 | ||||
| chr13:49110216-49110363 | Common:2; Rare:45 | ||||
| chr13:49247855-49247976 | Rare:39 | ||||
| chr13:49444117-49444439 | Rare:97 | ||||
| chr13:49585524-49585636 | Common:1; Rare:37 | ||||
| chr13:49691319-49691592 | Common:3; Rare:105 | ||||
| chr13:49792520-49792759 | Common:5; Rare:97 | ||||
| chr13:49996735-49997025 | Common:1; Rare:50 | ||||
| chr13:50081946-50082298 | Common:1; Rare:97 | ||||
| chr13:50909702-50910085 | Common:1; Rare:84; Clinvar:5; Clinvar (benign):1 |