| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrM:13005-13552 | |||||
| chrM:15524-15761 | |||||
| chrM:15883-15893 | |||||
| chrM:15919-16062 | |||||
| chrX:2609154-2609442 | Common:1; Rare:92 | ||||
| chrX:11351635-11351967 | Common:4; Rare:43 | ||||
| chrX:15675606-15675736 | Common:1; Rare:25 | ||||
| chrX:45770128-45770373 | Rare:17 | ||||
| chrX:55908055-55908250 | Rare:35 | ||||
| chrX:67545593-67545696 | Rare:26; Clinvar (pathogenic):1 | ||||
| chrX:73846558-73846645 | Common:1; Rare:18 | ||||
| chrX:74292494-74292743 | Rare:43 | ||||
| chrX:100645240-100645364 | Rare:16 | ||||
| chrX:100661903-100662211 | Common:3; Rare:59; Clinvar:2 | ||||
| chrX:100677051-100677126 | Rare:9 |