| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:48094997-48095209 | Common:1; Rare:106 | ||||
| chr13:48233089-48233475 | Common:2; Rare:132 | ||||
| chr13:48303665-48304048 | Common:1; Rare:126; Clinvar:15; Clinvar (benign):7; Clinvar (pathogenic):2 | ||||
| chr13:48444639-48444781 | Common:1; Rare:28 | ||||
| chr13:48533050-48533268 | Common:1; Rare:61 | ||||
| chr13:48975757-48976077 | Common:2; Rare:101 | ||||
| chr13:48976139-48976173 | Rare:11 | ||||
| chr13:48976564-48976666 | Rare:34 | ||||
| chr13:49110233-49110389 | Common:2; Rare:44 | ||||
| chr13:49247540-49247994 | Common:2; Rare:97 | ||||
| chr13:49413740-49413875 | Common:1; Rare:17 | ||||
| chr13:49443984-49444549 | Common:2; Rare:174 | ||||
| chr13:49495755-49496076 | Rare:75 | ||||
| chr13:49496102-49496456 | Common:4; Rare:81 | ||||
| chr13:49585471-49585658 | Common:1; Rare:67 |