| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:68074553-68074698 | Rare:60 | ||||
| chr10:68074720-68075020 | Common:2; Rare:155 | ||||
| chr10:68075063-68075587 | Common:23; Rare:823 | ||||
| chr10:68231234-68231860 | Common:3; Rare:442; Clinvar (pathogenic):6 | ||||
| chr10:68330872-68331350 | Common:7; Rare:218 | ||||
| chr10:68331367-68332232 | Common:16; Rare:1233 | ||||
| chr10:68332160-68332400 | Common:2; Rare:58 | ||||
| chr10:68332480-68332930 | Common:2; Rare:193 | ||||
| chr10:68332850-68333220 | Common:5; Rare:250 | ||||
| chr10:68406214-68407640 | Common:44; Rare:1276 | ||||
| chr10:68471540-68472320 | Common:14; Rare:932; Clinvar:3; Clinvar (benign):17 | ||||
| chr10:68527260-68527750 | Common:14; Rare:497; Clinvar (pathogenic):1 | ||||
| chr10:68559804-68560595 | Common:6; Rare:259 | ||||
| chr10:68560844-68561585 | Rare:167 | ||||
| chr10:68720652-68721414 | Common:15; Rare:754 |