| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:130330670-130330764 | Rare:16 | ||||
| chr9:133126261-133126484 | Common:1; Rare:38 | ||||
| chr9:133349553-133350302 | Common:1; Rare:273 | ||||
| chr9:136547401-136547629 | Common:2; Rare:64 | ||||
| chr9:136847931-136848016 | Rare:23 | ||||
| chr9:137223404-137223703 | Common:3; Rare:105 | ||||
| chrM:15866-15893 | |||||
| chrM:15937-16350 | |||||
| chrX:2609154-2609426 | Common:1; Rare:87 | ||||
| chrX:15675080-15675203 | Common:1; Rare:30 | ||||
| chrX:15675375-15675478 | Common:4; Rare:16 | ||||
| chrX:15675606-15675729 | Rare:23 | ||||
| chrX:24025663-24025732 | Rare:14 | ||||
| chrX:47214070-47214420 | Common:2; Rare:68; Clinvar:1; Clinvar (benign):1 | ||||
| chrX:49795309-49795625 | Rare:38 |