| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:97661769-97662083 | Common:3; Rare:42 | ||||
| chr9:98080573-98080970 | Rare:92; Clinvar (pathogenic):1 | ||||
| chr9:100004418-100004511 | Rare:23 | ||||
| chr9:100045404-100045416 | |||||
| chr9:100292111-100292401 | Rare:60; Clinvar:2 | ||||
| chr9:101486323-101486405 | Common:2; Rare:22 | ||||
| chr9:106859842-106860174 | Common:1; Rare:71 | ||||
| chr9:106860213-106860426 | Common:1; Rare:47 | ||||
| chr9:107637718-107638036 | Common:1; Rare:75 | ||||
| chr9:107712525-107712673 | Common:1; Rare:33 | ||||
| chr9:107751972-107752102 | Common:1; Rare:21 | ||||
| chr9:109251792-109251800 | Rare:1 | ||||
| chr9:109319255-109319367 | Rare:24 | ||||
| chr9:111039181-111039444 | Common:2; Rare:53 | ||||
| chr9:112170289-112170561 | Common:1; Rare:56 |