| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:57173551-57173867 | Common:2; Rare:112 | ||||
| chr5:58460070-58460228 | Common:4; Rare:59 | ||||
| chr5:60945056-60945235 | Common:4; Rare:62; Clinvar:2; Clinvar (benign):4 | ||||
| chr5:61162405-61162666 | Common:1; Rare:72 | ||||
| chr5:62412512-62412781 | Rare:86 | ||||
| chr5:64768598-64768960 | Common:4; Rare:95 | ||||
| chr5:65481870-65482097 | Common:1; Rare:34 | ||||
| chr5:65563116-65563313 | Common:3; Rare:70 | ||||
| chr5:65722093-65722223 | Common:1; Rare:46 | ||||
| chr5:66828766-66828814 | Rare:10 | ||||
| chr5:69166882-69167192 | Common:3; Rare:77 | ||||
| chr5:69189464-69189611 | Common:1; Rare:45 | ||||
| chr5:69369456-69369799 | Common:1; Rare:146 | ||||
| chr5:69369801-69369847 | Rare:17 | ||||
| chr5:71587152-71587391 | Common:1; Rare:80; Clinvar (benign):1 |