| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:136410611-136410666 | Rare:26 | ||||
| chr9:137618854-137619031 | Common:1; Rare:70 | ||||
| chrM:2468-3075 | |||||
| chrM:3204-3418 | |||||
| chrM:7907-8110 | |||||
| chrX:7148129-7148311 | Rare:51 | ||||
| chrX:11111141-11111356 | Common:3; Rare:45 | ||||
| chrX:13734604-13734811 | Common:3; Rare:69; Clinvar (benign):1 | ||||
| chrX:16719426-16719687 | Rare:71 | ||||
| chrX:16870227-16870685 | Common:3; Rare:106 | ||||
| chrX:23782950-23783199 | Common:4; Rare:51 | ||||
| chrX:38220813-38221044 | Rare:53 | ||||
| chrX:44542828-44543027 | Common:1; Rare:34 | ||||
| chrX:46545397-46545520 | Rare:21 | ||||
| chrX:47144668-47144812 | Rare:24 |