| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:133237434-133237788 | Rare:63 | ||||
| chr9:134963258-134963505 | Common:2; Rare:54 | ||||
| chr9:135089224-135089472 | Common:1; Rare:54 | ||||
| chr9:135480679-135480797 | Rare:25 | ||||
| chr9:136400133-136400328 | Common:2; Rare:66 | ||||
| chr9:136978035-136978260 | Rare:57 | ||||
| chr9:137129704-137129813 | Common:1; Rare:35 | ||||
| chr9:137223377-137223703 | Common:4; Rare:114 | ||||
| chr9:137449996-137450234 | Rare:87 | ||||
| chr9:137665864-137665975 | Rare:28 | ||||
| chrM:15765-15926 | |||||
| chrM:15937-16000 | |||||
| chrX:2609144-2609425 | Rare:90 | ||||
| chrX:10206418-10206770 | Rare:52; Clinvar:3; Clinvar (benign):1 | ||||
| chrX:15675128-15675478 | Common:8; Rare:62 |