| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:80459145-80459286 | Common:1; Rare:20 | ||||
| chr10:80459374-80459699 | Common:3; Rare:53 | ||||
| chr10:86521749-86521960 | Rare:69 | ||||
| chr10:86756258-86756648 | Common:4; Rare:133 | ||||
| chr10:86957553-86957797 | Rare:58 | ||||
| chr10:86968381-86968634 | Common:3; Rare:69 | ||||
| chr10:87094627-87094751 | Rare:49; Clinvar (benign):1 | ||||
| chr10:87094968-87095238 | Common:1; Rare:62 | ||||
| chr10:87504811-87504935 | Common:1; Rare:58 | ||||
| chr10:87659543-87659948 | Common:7; Rare:101 | ||||
| chr10:87660078-87660374 | Common:6; Rare:68 | ||||
| chr10:87818158-87818336 | Rare:66 | ||||
| chr10:87863276-87863665 | Common:2; Rare:132; Clinvar:80; Clinvar (benign):8 | ||||
| chr10:87864132-87864538 | Common:1; Rare:123; Clinvar:18; Clinvar (benign):11; Clinvar (pathogenic):1 | ||||
| chr10:88583196-88583521 | Rare:84 |