| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:121321005-121321433 | Common:3; Rare:101; Clinvar (benign):4 | ||||
| chr9:121324263-121324644 | Common:2; Rare:78 | ||||
| chr9:121331183-121331446 | Rare:42 | ||||
| chr9:121499688-121499806 | Rare:42 | ||||
| chr9:121557811-121558109 | Common:4; Rare:60 | ||||
| chr9:123076483-123076688 | Rare:49 | ||||
| chr9:124357476-124357716 | Common:1; Rare:39 | ||||
| chr9:125153662-125153951 | Common:2; Rare:60 | ||||
| chr9:126805805-126806051 | Common:1; Rare:57 | ||||
| chr9:127078488-127078585 | Common:1; Rare:15 | ||||
| chr9:127448358-127448513 | Rare:65 | ||||
| chr9:127507286-127507529 | Common:2; Rare:86 | ||||
| chr9:127817168-127817326 | Common:1; Rare:40; Clinvar:2; Clinvar (benign):5 | ||||
| chr9:127818803-127819006 | Rare:56; Clinvar:3 | ||||
| chr9:127819621-127819738 | Rare:37; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):3 |