| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:129607789-129607959 | Common:1; Rare:30 | ||||
| chr9:136839090-136839359 | Common:1; Rare:128 | ||||
| chrM:1486-1641 | |||||
| chrM:15369-15689 | |||||
| chrM:15809-15959 | |||||
| chrX:2609154-2609431 | Common:1; Rare:89 | ||||
| chrX:15675375-15675476 | Common:4; Rare:16 | ||||
| chrX:15675606-15675735 | Common:1; Rare:24 | ||||
| chrX:22136391-22136577 | Rare:24 | ||||
| chrX:38870586-38870747 | Common:3; Rare:25 | ||||
| chrX:44950931-44951159 | Common:3; Rare:24 | ||||
| chrX:45515382-45515659 | Common:2; Rare:40 | ||||
| chrX:45771223-45771396 | Rare:15 | ||||
| chrX:45851488-45851674 | Common:1; Rare:43 | ||||
| chrX:154362268-154362532 | Common:1; Rare:75; Clinvar:9; Clinvar (benign):7 |