| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:53481690-53482170 | Common:5; Rare:129 | ||||
| chr5:53601734-53601834 | Rare:24 | ||||
| chr5:55226509-55226645 | Rare:40; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:55232647-55233041 | Common:2; Rare:147 | ||||
| chr5:55234510-55234750 | Common:4; Rare:106 | ||||
| chr5:55601230-55601660 | Common:4; Rare:149 | ||||
| chr5:58259620-58259990 | Common:5; Rare:120 | ||||
| chr5:58891070-58891510 | Rare:165 | ||||
| chr5:59126450-59127100 | Common:2; Rare:157 | ||||
| chr5:59127171-59127417 | Common:3; Rare:51 | ||||
| chr5:59127570-59127830 | Common:6; Rare:87 | ||||
| chr5:59276922-59277165 | Rare:79 | ||||
| chr5:59301057-59301211 | Rare:26 | ||||
| chr5:59317310-59317656 | Common:2; Rare:77 | ||||
| chr5:59381800-59382050 | Common:1; Rare:42 |