| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:133356476-133356619 | Common:1; Rare:68; Clinvar (benign):2 | ||||
| chr9:133375965-133376369 | Common:3; Rare:146 | ||||
| chr9:133418040-133418133 | Common:2; Rare:17 | ||||
| chr9:133479088-133479329 | Common:1; Rare:70 | ||||
| chr9:134641478-134641845 | Common:2; Rare:111; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:134642108-134642293 | Common:4; Rare:58; Clinvar:7; Clinvar (benign):7 | ||||
| chr9:136410431-136410678 | Common:6; Rare:108 | ||||
| chr9:136848659-136848789 | Rare:38 | ||||
| chr9:136886245-136886534 | Common:2; Rare:87 | ||||
| chr9:136996539-136996762 | Common:2; Rare:65 | ||||
| chr9:137086811-137087176 | Common:2; Rare:153; Clinvar:6; Clinvar (benign):2 | ||||
| chr9:137188547-137188738 | Common:2; Rare:95 | ||||
| chr9:137205377-137205748 | Common:1; Rare:133 | ||||
| chr9:137551636-137551948 | Common:29; Rare:131 | ||||
| chr9:137618764-137619038 | Common:1; Rare:125 |