| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:144950592-144950932 | Common:5; Rare:110 | ||||
| chr8:145052133-145052537 | Common:11; Rare:117 | ||||
| chr9:178892-179125 | Common:7; Rare:60 | ||||
| chr9:470117-470331 | Common:16; Rare:94 | ||||
| chr9:504409-504726 | Common:4; Rare:155 | ||||
| chr9:2015062-2015387 | Common:3; Rare:96 | ||||
| chr9:2017387-2017435 | Rare:9 | ||||
| chr9:2181829-2182069 | Common:2; Rare:78 | ||||
| chr9:2621249-2621575 | Common:4; Rare:119 | ||||
| chr9:2621826-2622209 | Common:6; Rare:143; Clinvar:9; Clinvar (benign):4 | ||||
| chr9:2844049-2844363 | Common:6; Rare:124 | ||||
| chr9:3525472-3526172 | Common:2; Rare:253 | ||||
| chr9:3526420-3526741 | Common:4; Rare:148 | ||||
| chr9:4490343-4490682 | Common:1; Rare:117; Clinvar:5 | ||||
| chr9:4662172-4662361 | Common:3; Rare:78 |