| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:76444152-76444335 | Rare:31 | ||||
| chr10:79067410-79067454 | Common:1; Rare:15 | ||||
| chr10:79826204-79826889 | Common:5; Rare:208 | ||||
| chr10:80201547-80201819 | Common:1; Rare:50 | ||||
| chr10:80467983-80468301 | Common:2; Rare:67 | ||||
| chr10:86666585-86666856 | Common:1; Rare:61 | ||||
| chr10:86680098-86680383 | Common:3; Rare:70; Clinvar:2; Clinvar (benign):4 | ||||
| chr10:86682286-86682516 | Common:3; Rare:66 | ||||
| chr10:86686824-86686906 | Common:2; Rare:5 | ||||
| chr10:86706656-86706929 | Common:2; Rare:61; Clinvar:3; Clinvar (benign):6 | ||||
| chr10:86718104-86718178 | Common:1; Rare:17; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr10:86755585-86755894 | Common:1; Rare:71 | ||||
| chr10:86955568-86955791 | Rare:35 | ||||
| chr10:86970798-86971112 | Common:4; Rare:60 | ||||
| chr10:87342283-87342469 | Common:4; Rare:72 |