| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:443095-443263 | Common:8; Rare:75 | ||||
| chr5:693286-693586 | Common:6; Rare:88 | ||||
| chr5:892647-892897 | Common:5; Rare:85 | ||||
| chr5:1799778-1799986 | Common:8; Rare:98 | ||||
| chr5:1801286-1801455 | Common:4; Rare:85; Clinvar:3; Clinvar (benign):1 | ||||
| chr5:5422385-5422710 | Common:2; Rare:110 | ||||
| chr5:6378440-6378622 | Rare:81 | ||||
| chr5:6633017-6633087 | Common:2; Rare:28; Clinvar:1 | ||||
| chr5:7868991-7869204 | Common:2; Rare:109; Clinvar (benign):1 | ||||
| chr5:9546073-9546333 | Common:6; Rare:60 | ||||
| chr5:10353597-10353905 | Common:3; Rare:111 | ||||
| chr5:14664582-14664727 | Common:2; Rare:66 | ||||
| chr5:16465515-16465902 | Rare:106 | ||||
| chr5:16616985-16617195 | Common:2; Rare:57; Clinvar (benign):5 | ||||
| chr5:31532043-31532352 | Common:3; Rare:87 |