| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrM:8913-9163 | |||||
| chrM:9166-9433 | |||||
| chrM:9525-9548 | |||||
| chrM:9570-9842 | |||||
| chrM:10045-10119 | |||||
| chrM:11739-12139 | |||||
| chrM:12189-12244 | |||||
| chrM:14734-14955 | |||||
| chrX:281284-281504 | Common:2; Rare:51 | ||||
| chrX:1392059-1392356 | Common:6; Rare:127 | ||||
| chrX:2691151-2691494 | Common:9; Rare:150 | ||||
| chrX:11111103-11111388 | Common:4; Rare:60 | ||||
| chrX:11758196-11758625 | Common:2; Rare:78 | ||||
| chrX:13734584-13734859 | Common:3; Rare:82; Clinvar (benign):1 | ||||
| chrX:14029801-14029952 | Common:1; Rare:45 |