| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:15422578-15422881 | Common:1; Rare:128 | ||||
| chr9:19127467-19127581 | Common:1; Rare:36 | ||||
| chr9:19379489-19379891 | Common:1; Rare:137 | ||||
| chr9:19380191-19380349 | Common:4; Rare:77 | ||||
| chr9:20684113-20684282 | Common:2; Rare:64 | ||||
| chr9:21335369-21335515 | Common:2; Rare:52 | ||||
| chr9:21802441-21802677 | Common:2; Rare:63; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:21994350-21994579 | Rare:71; Clinvar:1; Clinvar (benign):4 | ||||
| chr9:21994598-21994714 | Common:1; Rare:30 | ||||
| chr9:26892738-26892866 | Rare:66 | ||||
| chr9:26947107-26947300 | Common:1; Rare:69 | ||||
| chr9:33001570-33001721 | Common:2; Rare:80; Clinvar (benign):3 | ||||
| chr9:33025090-33025363 | Common:7; Rare:117 | ||||
| chr9:34048870-34048992 | Common:1; Rare:49 | ||||
| chr9:34049178-34049263 | Common:1; Rare:21 |