| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:35489895-35490154 | Common:3; Rare:73 | ||||
| chr9:35563748-35563992 | Rare:74 | ||||
| chr9:35607900-35607952 | Common:1; Rare:14 | ||||
| chr9:35657724-35657816 | Common:2; Rare:73; Clinvar:11; Clinvar (benign):1; Clinvar (pathogenic):5 | ||||
| chr9:35657841-35658474 | Common:11; Rare:480; Clinvar:42; Clinvar (benign):16; Clinvar (pathogenic):40 | ||||
| chr9:35689702-35690129 | Common:4; Rare:132; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr9:35690610-35690938 | Rare:68 | ||||
| chr9:35691067-35691258 | Common:1; Rare:40 | ||||
| chr9:35698806-35699045 | Common:1; Rare:64 | ||||
| chr9:35703650-35703861 | Common:1; Rare:51 | ||||
| chr9:35732073-35732344 | Common:2; Rare:75 | ||||
| chr9:35732359-35732407 | Rare:15 | ||||
| chr9:35732410-35732683 | Common:3; Rare:67 | ||||
| chr9:35748982-35749379 | Common:2; Rare:147 | ||||
| chr9:35814945-35815302 | Rare:92 |