| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:73167473-73167775 | Common:1; Rare:48 | ||||
| chr10:73167899-73168691 | Common:2; Rare:197 | ||||
| chr10:73251727-73251934 | Rare:88; Clinvar (benign):1 | ||||
| chr10:73252364-73252879 | Common:3; Rare:153; Clinvar:5; Clinvar (benign):4 | ||||
| chr10:73252908-73253008 | Rare:22 | ||||
| chr10:73358404-73358522 | Rare:31 | ||||
| chr10:73358660-73358939 | Common:2; Rare:76 | ||||
| chr10:73413583-73413861 | Common:1; Rare:52 | ||||
| chr10:73413896-73414393 | Common:3; Rare:119 | ||||
| chr10:73414403-73414424 | Rare:4 | ||||
| chr10:73495557-73495831 | Rare:69 | ||||
| chr10:73495860-73496193 | Common:3; Rare:75 | ||||
| chr10:73591301-73591395 | Common:1; Rare:22 | ||||
| chr10:73592015-73592163 | Rare:28 | ||||
| chr10:73625092-73625200 | Rare:16 |