| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrM:7732-8592 | |||||
| chrM:8594-9049 | |||||
| chrM:9059-9803 | |||||
| chrM:9993-10149 | |||||
| chrM:10468-10737 | |||||
| chrM:12743-13008 | |||||
| chrX:7927379-7927512 | Common:1; Rare:33 | ||||
| chrX:7927697-7927760 | Rare:10 | ||||
| chrX:10156826-10156988 | Rare:21 | ||||
| chrX:11111134-11111356 | Common:3; Rare:48 | ||||
| chrX:13734543-13734854 | Common:3; Rare:94; Clinvar (benign):1 | ||||
| chrX:14873040-14873461 | Common:1; Rare:79 | ||||
| chrX:15335511-15335716 | Common:3; Rare:49; Clinvar (benign):1 | ||||
| chrX:16719426-16719678 | Rare:69 | ||||
| chrX:16786186-16786490 | Common:1; Rare:61 |