| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:185775255-185775496 | Common:1; Rare:39 | ||||
| chr4:186191414-186191823 | Common:12; Rare:248; Clinvar:4; Clinvar (benign):10 | ||||
| chr4:186723670-186724140 | Common:17; Rare:257 | ||||
| chr4:186726620-186726819 | Common:4; Rare:65 | ||||
| chr4:186726830-186727450 | Common:4; Rare:230 | ||||
| chr4:188109282-188110233 | Common:10; Rare:197 | ||||
| chr4:189940592-189940991 | Common:23; Rare:249 | ||||
| chr5:218087-218385 | Common:8; Rare:243; Clinvar:19; Clinvar (benign):14; Clinvar (pathogenic):4 | ||||
| chr5:225151-225516 | Common:4; Rare:179; Clinvar:18; Clinvar (benign):8; Clinvar (pathogenic):2 | ||||
| chr5:271029-271926 | Common:20; Rare:692 | ||||
| chr5:321513-321770 | Common:4; Rare:111 | ||||
| chr5:443056-443288 | Common:20; Rare:193 | ||||
| chr5:612082-612508 | Common:1; Rare:240 | ||||
| chr5:693270-693570 | Common:12; Rare:146 | ||||
| chr5:892480-893073 | Common:10; Rare:348 |