| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:21802461-21802668 | Common:2; Rare:57; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:22009244-22009476 | Common:1; Rare:77 | ||||
| chr9:26892738-26892827 | Rare:52 | ||||
| chr9:26947132-26947255 | Rare:44 | ||||
| chr9:26956267-26956459 | Common:2; Rare:73 | ||||
| chr9:27529751-27529968 | Common:4; Rare:61 | ||||
| chr9:32384451-32384721 | Common:1; Rare:95 | ||||
| chr9:32552059-32552358 | Common:2; Rare:83 | ||||
| chr9:32552557-32552644 | Common:1; Rare:16; Clinvar:2 | ||||
| chr9:32573073-32573193 | Common:2; Rare:47 | ||||
| chr9:33001543-33001746 | Common:3; Rare:102; Clinvar (benign):4 | ||||
| chr9:33025093-33025383 | Common:6; Rare:120 | ||||
| chr9:33076612-33076850 | Common:2; Rare:81 | ||||
| chr9:33166779-33166951 | Rare:61; Clinvar:2 | ||||
| chr9:33290369-33290570 | Common:2; Rare:78 |