| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrM:10468-10971 | |||||
| chrM:12263-12366 | |||||
| chrM:12669-12849 | |||||
| chrM:14149-14469 | |||||
| chrM:15049-15133 | |||||
| chrM:15138-15183 | |||||
| chrX:1392100-1392371 | Common:6; Rare:117 | ||||
| chrX:11111202-11111356 | Common:3; Rare:31 | ||||
| chrX:11759345-11759649 | Common:2; Rare:47 | ||||
| chrX:13734551-13734832 | Common:3; Rare:86; Clinvar (benign):1 | ||||
| chrX:14873049-14873513 | Common:2; Rare:90 | ||||
| chrX:16719410-16719655 | Rare:61 | ||||
| chrX:17737209-17737505 | Common:3; Rare:27 | ||||
| chrX:20141780-20142124 | Common:1; Rare:74 | ||||
| chrX:23907891-23908136 | Rare:54 |