| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:144700502-144700682 | Common:2; Rare:39 | ||||
| chr8:145002825-145003045 | Common:2; Rare:79 | ||||
| chr9:9441775-9442077 | Common:5; Rare:82 | ||||
| chr9:15468760-15469028 | Rare:77 | ||||
| chr9:15469030-15469365 | Common:2; Rare:110 | ||||
| chr9:16575342-16575529 | Common:1; Rare:50 | ||||
| chr9:16726874-16726913 | Rare:9 | ||||
| chr9:17906467-17906811 | Common:1; Rare:125 | ||||
| chr9:32550831-32551142 | Common:1; Rare:126; Clinvar:2; Clinvar (benign):2 | ||||
| chr9:35604225-35604378 | Rare:36 | ||||
| chr9:35657531-35657766 | Common:1; Rare:76; Clinvar:6; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr9:35706768-35707154 | Common:2; Rare:111 | ||||
| chr9:39809851-39809865 | Common:1 | ||||
| chr9:40991980-40992420 | Common:7; Rare:30 | ||||
| chr9:62897955-62898207 | Common:5; Rare:49 |