| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrM:7400-7586 | |||||
| chrM:7916-8152 | |||||
| chrM:10354-10504 | |||||
| chrM:10807-11060 | |||||
| chrM:14590-15163 | |||||
| chrX:276229-276375 | Common:3; Rare:50 | ||||
| chrX:1392093-1392376 | Common:6; Rare:121 | ||||
| chrX:2964309-2964498 | Common:1; Rare:28 | ||||
| chrX:7148120-7148304 | Common:1; Rare:54 | ||||
| chrX:11111165-11111362 | Common:3; Rare:40 | ||||
| chrX:12974988-12975168 | Common:2; Rare:45 | ||||
| chrX:13734540-13734848 | Common:3; Rare:94; Clinvar (benign):1 | ||||
| chrX:14873034-14873431 | Common:1; Rare:73 | ||||
| chrX:15493230-15493437 | Common:1; Rare:33 | ||||
| chrX:16719468-16719683 | Rare:66 |