| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:135499833-135499970 | Common:3; Rare:41 | ||||
| chr9:135961111-135961547 | Common:7; Rare:155 | ||||
| chr9:136410603-136410686 | Rare:44 | ||||
| chr9:136849545-136849787 | Common:1; Rare:91 | ||||
| chr9:136886250-136886533 | Common:2; Rare:83 | ||||
| chr9:136944604-136944937 | Common:2; Rare:125 | ||||
| chr9:137086698-137087014 | Common:1; Rare:119; Clinvar:2; Clinvar (benign):1 | ||||
| chr9:137188538-137188744 | Common:2; Rare:101 | ||||
| chr9:137205376-137205772 | Common:1; Rare:151 | ||||
| chr9:137551618-137551953 | Common:29; Rare:141 | ||||
| chr9:137578864-137579009 | Common:2; Rare:48 | ||||
| chr9:137618758-137619035 | Common:1; Rare:124 | ||||
| chrM:3167-3437 | |||||
| chrM:3475-3664 | |||||
| chrM:4297-4569 |