| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:18473941-18474163 | Rare:58 | ||||
| chr9:21994224-21994885 | Common:2; Rare:203; Clinvar:13; Clinvar (benign):13; Clinvar (pathogenic):2 | ||||
| chr9:21994923-21995046 | Common:1; Rare:20 | ||||
| chr9:26892332-26892517 | Rare:86 | ||||
| chr9:33001579-33001769 | Common:3; Rare:88; Clinvar (benign):3 | ||||
| chr9:33025093-33025304 | Common:5; Rare:89 | ||||
| chr9:33264672-33265081 | Common:1; Rare:111 | ||||
| chr9:34049185-34049267 | Common:1; Rare:19 | ||||
| chr9:34329210-34329593 | Rare:120 | ||||
| chr9:35102771-35103225 | Common:1; Rare:139 | ||||
| chr9:35658018-35658337 | Common:6; Rare:210; Clinvar:15; Clinvar (benign):10; Clinvar (pathogenic):24 | ||||
| chr9:35665190-35665318 | Common:2; Rare:45 | ||||
| chr9:35689706-35689999 | Common:3; Rare:96; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr9:35732080-35732356 | Common:2; Rare:83 | ||||
| chr9:35732372-35732683 | Common:3; Rare:78 |