| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:125239137-125239502 | Rare:68 | ||||
| chr9:127448410-127448498 | Rare:44 | ||||
| chr9:127810790-127810978 | Rare:39 | ||||
| chr9:127816983-127817193 | Rare:57; Clinvar:3; Clinvar (benign):1 | ||||
| chr9:127818773-127819031 | Common:1; Rare:63; Clinvar:3 | ||||
| chr9:127819621-127819787 | Rare:46; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):3 | ||||
| chr9:127819960-127820260 | Rare:58; Clinvar:1 | ||||
| chr9:127825779-127825951 | Common:2; Rare:55; Clinvar:6; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
| chr9:127826664-127826687 | Rare:6; Clinvar:1 | ||||
| chr9:128258059-128258483 | Common:3; Rare:117 | ||||
| chr9:128883012-128883189 | Common:1; Rare:41 | ||||
| chr9:129176878-129177169 | Common:1; Rare:116 | ||||
| chr9:129320836-129321017 | Rare:28 | ||||
| chr9:129496716-129496935 | Common:2; Rare:67 | ||||
| chr9:129607788-129607959 | Common:1; Rare:30 |