| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:35690595-35690938 | Rare:70 | ||||
| chr9:35691067-35691265 | Common:1; Rare:42 | ||||
| chr9:35703561-35703898 | Common:1; Rare:82 | ||||
| chr9:35704330-35704814 | Common:1; Rare:115 | ||||
| chr9:35706471-35707154 | Common:2; Rare:185 | ||||
| chr9:35732073-35732334 | Common:2; Rare:70 | ||||
| chr9:35732358-35732684 | Common:3; Rare:84 | ||||
| chr9:35748941-35749368 | Common:2; Rare:152 | ||||
| chr9:35814976-35815270 | Rare:73 | ||||
| chr9:35829113-35829280 | Common:1; Rare:45 | ||||
| chr9:35906088-35906290 | Rare:50 | ||||
| chr9:36190731-36191225 | Common:3; Rare:157 | ||||
| chr9:36258375-36258625 | Common:2; Rare:60; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:36400837-36400986 | Common:3; Rare:71 | ||||
| chr9:37592502-37592679 | Common:2; Rare:64 |