| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:218114-218349 | Common:2; Rare:91; Clinvar:1; Clinvar (benign):2 | ||||
| chr5:443063-443272 | Common:10; Rare:93 | ||||
| chr5:892731-892999 | Common:2; Rare:106 | ||||
| chr5:1799770-1799961 | Common:8; Rare:94 | ||||
| chr5:1801300-1801527 | Common:4; Rare:120; Clinvar:3; Clinvar (benign):3 | ||||
| chr5:6378456-6378678 | Rare:90 | ||||
| chr5:6632959-6633460 | Common:8; Rare:158; Clinvar:10; Clinvar (benign):4 | ||||
| chr5:7868997-7869227 | Common:2; Rare:120; Clinvar:1; Clinvar (benign):3 | ||||
| chr5:9546069-9546347 | Common:7; Rare:65 | ||||
| chr5:10249874-10250160 | Common:16; Rare:138 | ||||
| chr5:10353579-10353905 | Common:3; Rare:124 | ||||
| chr5:10441813-10441898 | Rare:23 | ||||
| chr5:14418473-14418665 | Common:2; Rare:37 | ||||
| chr5:16465164-16465306 | Rare:44 | ||||
| chr5:31532040-31532362 | Common:3; Rare:94 |