| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:132669939-132670046 | Common:1; Rare:52 | ||||
| chr9:132670390-132670496 | Rare:33 | ||||
| chr9:132878264-132878370 | Common:1; Rare:40 | ||||
| chr9:133030465-133030759 | Common:4; Rare:83 | ||||
| chr9:133348033-133348280 | Common:3; Rare:104 | ||||
| chr9:133356454-133356593 | Common:1; Rare:63; Clinvar (benign):2 | ||||
| chr9:133375955-133376366 | Common:3; Rare:148 | ||||
| chr9:133417953-133418312 | Common:4; Rare:85 | ||||
| chr9:134135781-134136135 | Common:4; Rare:101 | ||||
| chr9:134641523-134641913 | Common:2; Rare:107; Clinvar:2; Clinvar (benign):1 | ||||
| chr9:136118811-136119005 | Common:4; Rare:85 | ||||
| chr9:136327230-136327636 | Common:6; Rare:138 | ||||
| chr9:136410460-136410695 | Common:7; Rare:115 | ||||
| chr9:136546043-136546217 | Rare:75 | ||||
| chr9:136807744-136807952 | Common:1; Rare:87 |