| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:34653663-34653929 | Rare:43 | ||||
| chr9:34665344-34665665 | Rare:98 | ||||
| chr9:34665921-34666174 | Common:2; Rare:63 | ||||
| chr9:34729445-34729641 | Common:1; Rare:32 | ||||
| chr9:34895725-34895967 | Common:1; Rare:37 | ||||
| chr9:34989479-34989790 | Common:2; Rare:81 | ||||
| chr9:35040965-35041135 | Rare:35 | ||||
| chr9:35041937-35042282 | Rare:70 | ||||
| chr9:35042358-35042399 | Rare:11 | ||||
| chr9:35059206-35059794 | Rare:118; Clinvar:4; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr9:35071938-35072480 | Common:1; Rare:172; Clinvar:1 | ||||
| chr9:35072482-35072675 | Rare:52; Clinvar:3; Clinvar (benign):1 | ||||
| chr9:35072683-35072895 | Rare:44; Clinvar:1 | ||||
| chr9:35079723-35079758 | Rare:4 | ||||
| chr9:35079996-35080107 | Common:3; Rare:26; Clinvar:2; Clinvar (benign):2 |