| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:35162262-35162296 | Rare:14 | ||||
| chr9:35657846-35658376 | Common:8; Rare:441; Clinvar:42; Clinvar (benign):15; Clinvar (pathogenic):40 | ||||
| chr9:35665176-35665313 | Common:1; Rare:50 | ||||
| chr9:35689702-35690130 | Common:4; Rare:133; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr9:35691088-35691255 | Common:1; Rare:36 | ||||
| chr9:35732074-35732344 | Common:2; Rare:75 | ||||
| chr9:35732353-35732684 | Common:3; Rare:86 | ||||
| chr9:35748982-35749365 | Common:2; Rare:142 | ||||
| chr9:35814963-35815279 | Rare:78 | ||||
| chr9:36190738-36191129 | Common:2; Rare:130 | ||||
| chr9:36258374-36258576 | Common:1; Rare:47; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:36276958-36277308 | Common:2; Rare:74; Clinvar:3 | ||||
| chr9:36400833-36400997 | Common:3; Rare:71 | ||||
| chr9:37422611-37422753 | Common:2; Rare:73 | ||||
| chr9:37465271-37465522 | Common:3; Rare:85 |