| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:73865770-73866110 | Common:2; Rare:87 | ||||
| chr10:73875179-73875440 | Rare:112 | ||||
| chr10:73888890-73889480 | Common:3; Rare:170 | ||||
| chr10:73932370-73932870 | Rare:159 | ||||
| chr10:73956570-73956855 | Common:3; Rare:53 | ||||
| chr10:73956980-73957104 | Common:1; Rare:21 | ||||
| chr10:73958569-73958714 | Common:3; Rare:25 | ||||
| chr10:73979798-73980198 | Common:1; Rare:91 | ||||
| chr10:74095536-74095936 | Common:1; Rare:177; Clinvar:19; Clinvar (benign):22; Clinvar (pathogenic):4 | ||||
| chr10:74117710-74118120 | Common:1; Rare:130; Clinvar:2; Clinvar (benign):4 | ||||
| chr10:74152171-74152571 | Common:4; Rare:74 | ||||
| chr10:74156998-74157132 | Common:1; Rare:16 | ||||
| chr10:74165508-74165908 | Common:3; Rare:73 | ||||
| chr10:74166510-74166910 | Common:10; Rare:70 | ||||
| chr10:74177232-74177758 | Rare:132 |