| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:92412625-92412891 | Rare:40 | ||||
| chr9:95037999-95038266 | Rare:61 | ||||
| chr9:95083114-95083566 | Common:5; Rare:142 | ||||
| chr9:95106895-95107021 | Common:1; Rare:24; Clinvar (benign):1 | ||||
| chr9:95111461-95111885 | Common:2; Rare:114; Clinvar:16; Clinvar (benign):13; Clinvar (pathogenic):4 | ||||
| chr9:95117393-95117657 | Common:1; Rare:63; Clinvar (benign):2 | ||||
| chr9:95120980-95121161 | Rare:26 | ||||
| chr9:95123578-95123684 | Rare:32 | ||||
| chr9:95129810-95130158 | Rare:70 | ||||
| chr9:96464009-96464147 | Rare:30 | ||||
| chr9:97238411-97238504 | Common:1; Rare:26 | ||||
| chr9:97593381-97593606 | Common:1; Rare:35 | ||||
| chr9:97606549-97606723 | Common:1; Rare:36 | ||||
| chr9:97687182-97687443 | Common:1; Rare:61; Clinvar:1; Clinvar (pathogenic):2 | ||||
| chr9:100057820-100057987 | Rare:39 |