| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:63521742-63522138 | Common:4; Rare:119 | ||||
| chr10:63522243-63522279 | Rare:8 | ||||
| chr10:63522284-63522352 | Rare:10 | ||||
| chr10:67884194-67884847 | Common:6; Rare:201 | ||||
| chr10:67884913-67885236 | Common:2; Rare:118 | ||||
| chr10:67885278-67885379 | Rare:32 | ||||
| chr10:68074613-68075516 | Common:8; Rare:263 | ||||
| chr10:68231374-68231795 | Common:1; Rare:136; Clinvar (pathogenic):2 | ||||
| chr10:68331043-68331114 | Rare:17 | ||||
| chr10:68331420-68332189 | Common:3; Rare:235 | ||||
| chr10:68332471-68333041 | Common:2; Rare:164 | ||||
| chr10:68406437-68406646 | Rare:53 | ||||
| chr10:68406747-68406831 | Rare:34 | ||||
| chr10:68406850-68407082 | Common:1; Rare:70 | ||||
| chr10:68407127-68407525 | Common:7; Rare:117 |