| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:186191472-186191814 | Common:6; Rare:113; Clinvar:2; Clinvar (benign):5 | ||||
| chr4:186723775-186723914 | Common:4; Rare:55 | ||||
| chr4:189940616-189941004 | Common:14; Rare:138 | ||||
| chr5:218114-218379 | Common:3; Rare:115; Clinvar:9; Clinvar (benign):8; Clinvar (pathogenic):2 | ||||
| chr5:443050-443284 | Common:10; Rare:104 | ||||
| chr5:612211-612357 | Rare:58 | ||||
| chr5:892512-893013 | Common:5; Rare:161 | ||||
| chr5:1799778-1799988 | Common:8; Rare:99 | ||||
| chr5:1801300-1801460 | Common:4; Rare:80; Clinvar:3; Clinvar (benign):1 | ||||
| chr5:2752232-2752253 | Rare:5 | ||||
| chr5:6378479-6378674 | Rare:81 | ||||
| chr5:6632982-6633398 | Common:8; Rare:134; Clinvar:10; Clinvar (benign):4 | ||||
| chr5:7868987-7869204 | Common:2; Rare:112; Clinvar (benign):1 | ||||
| chr5:9546006-9546362 | Common:9; Rare:90 | ||||
| chr5:10249856-10250528 | Common:19; Rare:313; Clinvar:5; Clinvar (benign):2 |