| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:103415090-103415476 | Common:6; Rare:200 | ||||
| chr8:109334078-109334396 | Common:1; Rare:79 | ||||
| chr8:120445097-120445431 | Common:1; Rare:80 | ||||
| chr8:124539054-124539181 | Common:1; Rare:68; Clinvar (benign):5 | ||||
| chr8:144792356-144792550 | Common:2; Rare:73 | ||||
| chr9:5437832-5438073 | Common:2; Rare:78 | ||||
| chr9:26947169-26947260 | Rare:30 | ||||
| chr9:33025093-33025304 | Common:5; Rare:89 | ||||
| chr9:33290383-33290551 | Common:2; Rare:62 | ||||
| chr9:34329270-34329592 | Rare:88 | ||||
| chr9:35657970-35658313 | Common:5; Rare:269; Clinvar:20; Clinvar (benign):11; Clinvar (pathogenic):34 | ||||
| chr9:35732182-35732676 | Common:3; Rare:134 | ||||
| chr9:36190725-36190978 | Common:1; Rare:83 | ||||
| chr9:37904103-37904198 | Rare:28 | ||||
| chr9:69759945-69760123 | Common:2; Rare:84 |