| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:121321025-121321401 | Common:3; Rare:89; Clinvar (benign):4 | ||||
| chr9:121498876-121498964 | Common:1; Rare:11 | ||||
| chr9:121499649-121499827 | Rare:55 | ||||
| chr9:127078488-127078508 | Rare:6 | ||||
| chr9:129174814-129175006 | Rare:43 | ||||
| chr9:129320877-129321013 | Rare:18 | ||||
| chr9:129413719-129413940 | Common:2; Rare:86 | ||||
| chr9:129488534-129488824 | Common:1; Rare:82 | ||||
| chr9:129698466-129698760 | Common:2; Rare:48 | ||||
| chr9:130712903-130713044 | Common:1; Rare:49 | ||||
| chr9:131373410-131373671 | Common:1; Rare:58 | ||||
| chr9:131668435-131668581 | Rare:27 | ||||
| chr9:136728182-136728480 | Common:4; Rare:98 | ||||
| chr9:136839444-136839776 | Common:1; Rare:127 | ||||
| chr9:137223393-137223703 | Common:3; Rare:108 |