| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:125889616-125889913 | Common:1; Rare:79 | ||||
| chr9:126338301-126338339 | Rare:8 | ||||
| chr9:126591842-126592050 | Rare:46 | ||||
| chr9:127448377-127448530 | Rare:66 | ||||
| chr9:127776435-127776571 | Common:2; Rare:24 | ||||
| chr9:127777077-127777249 | Rare:32 | ||||
| chr9:127815944-127816210 | Common:3; Rare:66; Clinvar:4; Clinvar (benign):4 | ||||
| chr9:127818330-127818590 | Common:1; Rare:60; Clinvar:2; Clinvar (benign):4 | ||||
| chr9:127819624-127819744 | Rare:37; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
| chr9:127829055-127829226 | Common:1; Rare:21 | ||||
| chr9:128156906-128157075 | Rare:23 | ||||
| chr9:128192941-128193050 | Common:4; Rare:30 | ||||
| chr9:128472812-128473044 | Common:4; Rare:59 | ||||
| chr9:128473064-128473258 | Common:1; Rare:51 | ||||
| chr9:128613194-128613485 | Common:1; Rare:55; Clinvar (benign):4 |