| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:125189753-125190046 | Common:1; Rare:114 | ||||
| chr9:125200287-125200590 | Common:1; Rare:102 | ||||
| chr9:126860565-126860711 | Common:2; Rare:48 | ||||
| chr9:127451261-127451520 | Common:2; Rare:112 | ||||
| chr9:127579003-127579305 | Common:4; Rare:60 | ||||
| chr9:127786368-127786481 | Rare:38 | ||||
| chr9:127802719-127802985 | Common:2; Rare:69 | ||||
| chr9:127899518-127899716 | Rare:71 | ||||
| chr9:128098262-128098538 | Common:1; Rare:55 | ||||
| chr9:128191750-128191839 | Common:1; Rare:23 | ||||
| chr9:128275909-128276307 | Common:5; Rare:173 | ||||
| chr9:128322414-128322551 | Common:1; Rare:42 | ||||
| chr9:128322735-128322887 | Common:2; Rare:70; Clinvar (benign):5 | ||||
| chr9:128371199-128371401 | Rare:75 | ||||
| chr9:128504601-128504805 | Rare:96; Clinvar:5 |