| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:185425877-185426255 | Common:6; Rare:158 | ||||
| chr4:185810809-185811450 | Common:7; Rare:168 | ||||
| chr4:186191403-186191825 | Common:12; Rare:255; Clinvar:4; Clinvar (benign):10 | ||||
| chr4:186265737-186265972 | Common:2; Rare:95; Clinvar:4 | ||||
| chr4:186723700-186723997 | Common:14; Rare:184 | ||||
| chr4:186726574-186726819 | Common:8; Rare:142 | ||||
| chr4:189940640-189940951 | Common:15; Rare:149 | ||||
| chr5:218106-218372 | Common:7; Rare:208; Clinvar:12; Clinvar (benign):10; Clinvar (pathogenic):2 | ||||
| chr5:443080-443278 | Common:20; Rare:180 | ||||
| chr5:612168-612359 | Rare:144 | ||||
| chr5:693320-693570 | Common:6; Rare:72 | ||||
| chr5:850497-850897 | Common:17; Rare:283 | ||||
| chr5:891251-891443 | Common:4; Rare:122 | ||||
| chr5:892513-892955 | Common:7; Rare:218 | ||||
| chr5:1112006-1112114 | Rare:45 |