| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:133356458-133356630 | Common:1; Rare:81; Clinvar (benign):2 | ||||
| chr9:133375995-133376366 | Common:2; Rare:134 | ||||
| chr9:133417861-133418324 | Common:5; Rare:132 | ||||
| chr9:134641547-134641771 | Common:1; Rare:66 | ||||
| chr9:136410333-136410671 | Common:6; Rare:141 | ||||
| chr9:136662707-136662972 | Common:1; Rare:66 | ||||
| chr9:136952413-136952646 | Common:1; Rare:52 | ||||
| chr9:137028162-137028495 | Common:1; Rare:99 | ||||
| chr9:137086832-137087102 | Rare:111; Clinvar:4; Clinvar (benign):1 | ||||
| chr9:137188547-137188723 | Common:2; Rare:90 | ||||
| chr9:137205368-137205723 | Common:1; Rare:121 | ||||
| chr9:137227203-137227519 | Common:1; Rare:66 | ||||
| chr9:137550372-137550511 | Rare:22 | ||||
| chr9:137618797-137619046 | Common:1; Rare:113 | ||||
| chrM:4057-4263 |