| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:88388276-88388527 | Common:1; Rare:114 | ||||
| chr9:88991321-88991512 | Common:2; Rare:51 | ||||
| chr9:89310898-89311205 | Common:2; Rare:92 | ||||
| chr9:89318409-89318569 | Common:5; Rare:76 | ||||
| chr9:92115339-92115492 | Common:1; Rare:49; Clinvar:1 | ||||
| chr9:92293522-92293907 | Common:6; Rare:117 | ||||
| chr9:92325296-92326001 | Common:9; Rare:192 | ||||
| chr9:92669996-92670424 | Common:1; Rare:137 | ||||
| chr9:92877969-92878253 | Common:2; Rare:75 | ||||
| chr9:93134233-93134349 | Common:2; Rare:44 | ||||
| chr9:93453546-93453698 | Rare:35 | ||||
| chr9:94921108-94921255 | Rare:26 | ||||
| chr9:95004124-95004203 | Rare:23 | ||||
| chr9:95317675-95317839 | Common:1; Rare:48; Clinvar:1 | ||||
| chr9:95506585-95506668 | Rare:38; Clinvar:4; Clinvar (benign):5 |