| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:128771847-128772035 | Rare:50 | ||||
| chr9:128881902-128882197 | Common:2; Rare:96 | ||||
| chr9:128882526-128882634 | Common:1; Rare:26 | ||||
| chr9:128922004-128922340 | Common:2; Rare:81 | ||||
| chr9:128947494-128947735 | Common:1; Rare:104; Clinvar:7; Clinvar (benign):1 | ||||
| chr9:129098114-129098365 | Common:1; Rare:81 | ||||
| chr9:129110642-129111029 | Common:5; Rare:119 | ||||
| chr9:129111217-129111468 | Common:2; Rare:85 | ||||
| chr9:129139361-129139511 | Common:2; Rare:36 | ||||
| chr9:129139897-129140145 | Rare:54 | ||||
| chr9:129141497-129141801 | Common:3; Rare:97 | ||||
| chr9:129628265-129628502 | Common:1; Rare:36 | ||||
| chr9:129753028-129753198 | Rare:43 | ||||
| chr9:129818583-129818749 | Common:1; Rare:47; Clinvar (benign):2 | ||||
| chr9:129824087-129824299 | Common:3; Rare:59; Clinvar:2; Clinvar (benign):2 |