| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:33264927-33265141 | Rare:66 | ||||
| chr9:33290367-33290570 | Common:2; Rare:79 | ||||
| chr9:33817633-33817890 | Common:1; Rare:72 | ||||
| chr9:34048866-34049267 | Common:2; Rare:128 | ||||
| chr9:34126375-34126409 | Rare:13 | ||||
| chr9:34329213-34329598 | Rare:119 | ||||
| chr9:34652015-34652213 | Rare:57 | ||||
| chr9:34665367-34665660 | Rare:96 | ||||
| chr9:35072388-35072675 | Rare:75; Clinvar:4; Clinvar (benign):1 | ||||
| chr9:35101206-35101453 | Common:1; Rare:74 | ||||
| chr9:35162262-35162451 | Rare:54 | ||||
| chr9:35657724-35657817 | Common:2; Rare:74; Clinvar:11; Clinvar (benign):1; Clinvar (pathogenic):5 | ||||
| chr9:35657841-35658496 | Common:11; Rare:483; Clinvar:42; Clinvar (benign):16; Clinvar (pathogenic):40 | ||||
| chr9:35685386-35685789 | Common:1; Rare:99; Clinvar:1; Clinvar (benign):5; Clinvar (pathogenic):2 | ||||
| chr9:35689702-35690173 | Common:4; Rare:142; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):1 |