| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:250733-251070 | Common:3; Rare:93; Clinvar:12; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr5:443084-443280 | Common:10; Rare:91 | ||||
| chr5:524447-524680 | Common:2; Rare:62 | ||||
| chr5:612197-612357 | Rare:64 | ||||
| chr5:693287-693540 | Common:6; Rare:75 | ||||
| chr5:892540-892923 | Common:5; Rare:118 | ||||
| chr5:1201337-1201653 | Common:5; Rare:111 | ||||
| chr5:1799791-1799988 | Common:4; Rare:92 | ||||
| chr5:1801300-1801549 | Common:4; Rare:129; Clinvar:3; Clinvar (benign):3 | ||||
| chr5:5422360-5422706 | Common:2; Rare:114 | ||||
| chr5:6378498-6378694 | Rare:79 | ||||
| chr5:6632937-6633429 | Common:10; Rare:158; Clinvar:10; Clinvar (benign):6 | ||||
| chr5:7868987-7869209 | Common:2; Rare:115; Clinvar (benign):1 | ||||
| chr5:9545628-9545749 | Rare:27 | ||||
| chr5:9546042-9546372 | Common:7; Rare:74 |