| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:96655296-96655368 | Rare:22 | ||||
| chr9:96778057-96778154 | Rare:30 | ||||
| chr9:97039051-97039337 | Common:1; Rare:108 | ||||
| chr9:97411869-97412236 | Common:4; Rare:107; Clinvar:2; Clinvar (benign):1 | ||||
| chr9:97633271-97633632 | Common:3; Rare:110 | ||||
| chr9:97633686-97633864 | Common:2; Rare:61 | ||||
| chr9:97697275-97697421 | Common:1; Rare:91; Clinvar:5; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr9:97922167-97922285 | Common:1; Rare:38 | ||||
| chr9:97922397-97922622 | Common:5; Rare:108 | ||||
| chr9:97983146-97983603 | Common:2; Rare:170 | ||||
| chr9:97984222-97984616 | Common:1; Rare:168 | ||||
| chr9:98056529-98056810 | Common:2; Rare:101 | ||||
| chr9:98255637-98255849 | Common:3; Rare:69 | ||||
| chr9:99104888-99105043 | Rare:43 | ||||
| chr9:99221906-99222371 | Common:2; Rare:185; Clinvar:3; Clinvar (benign):2 |