| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:133417901-133418319 | Common:5; Rare:104 | ||||
| chr9:133459901-133460044 | Common:1; Rare:64 | ||||
| chr9:133479088-133479338 | Common:1; Rare:71 | ||||
| chr9:136410391-136410686 | Common:6; Rare:128 | ||||
| chr9:136944604-136944873 | Common:2; Rare:104 | ||||
| chr9:137028201-137028425 | Rare:66 | ||||
| chr9:137086631-137087146 | Common:2; Rare:213; Clinvar:6; Clinvar (benign):1 | ||||
| chr9:137138155-137138376 | Common:1; Rare:32 | ||||
| chr9:137188538-137188723 | Common:2; Rare:93 | ||||
| chr9:137205389-137205757 | Common:1; Rare:136 | ||||
| chr9:137423137-137423532 | Common:3; Rare:123 | ||||
| chr9:137551647-137551965 | Common:28; Rare:135 | ||||
| chr9:137618797-137619047 | Common:1; Rare:113 | ||||
| chrM:3169-3531 | |||||
| chrM:4327-4621 |