| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:60945038-60945263 | Common:4; Rare:84; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr5:61162372-61162499 | Common:1; Rare:29 | ||||
| chr5:62403844-62404030 | Common:3; Rare:64 | ||||
| chr5:62412557-62412784 | Rare:73 | ||||
| chr5:64768559-64768977 | Common:5; Rare:110 | ||||
| chr5:65481829-65481981 | Common:1; Rare:26 | ||||
| chr5:65563109-65563406 | Common:4; Rare:117 | ||||
| chr5:65624626-65624758 | Common:9; Rare:20 | ||||
| chr5:65624981-65625058 | Rare:26 | ||||
| chr5:65722051-65722329 | Common:4; Rare:92 | ||||
| chr5:65926610-65926760 | Common:4; Rare:44 | ||||
| chr5:66144175-66144351 | Common:2; Rare:59 | ||||
| chr5:67004055-67004297 | Common:3; Rare:87 | ||||
| chr5:67004429-67004701 | Common:1; Rare:74 | ||||
| chr5:68215553-68215774 | Common:4; Rare:74 |