| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:33473843-33474143 | Common:4; Rare:93 | ||||
| chr9:33817526-33817928 | Common:2; Rare:112 | ||||
| chr9:34048825-34048995 | Common:2; Rare:74 | ||||
| chr9:34049186-34049267 | Common:1; Rare:19 | ||||
| chr9:34329206-34329606 | Rare:125 | ||||
| chr9:34652015-34652218 | Rare:59 | ||||
| chr9:34665373-34665665 | Rare:94 | ||||
| chr9:34665977-34666238 | Common:3; Rare:69 | ||||
| chr9:35072336-35072675 | Rare:90; Clinvar:4; Clinvar (benign):1 | ||||
| chr9:35162277-35162408 | Rare:37 | ||||
| chr9:35489779-35490144 | Common:3; Rare:115 | ||||
| chr9:35607900-35607946 | Common:1; Rare:14 | ||||
| chr9:35657841-35658495 | Common:11; Rare:483; Clinvar:42; Clinvar (benign):16; Clinvar (pathogenic):40 | ||||
| chr9:35673886-35673928 | Common:2; Rare:12 | ||||
| chr9:35685426-35685789 | Common:1; Rare:85; Clinvar:1; Clinvar (benign):5; Clinvar (pathogenic):2 |