| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:43515118-43515175 | Common:1; Rare:22 | ||||
| chr5:43602418-43602736 | Common:2; Rare:52 | ||||
| chr5:43603061-43603285 | Rare:56 | ||||
| chr5:44808727-44809111 | Common:4; Rare:149 | ||||
| chr5:50667493-50667576 | Rare:32 | ||||
| chr5:52989229-52989409 | Common:4; Rare:49; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:53109716-53109923 | Common:1; Rare:104; Clinvar:3 | ||||
| chr5:54310434-54310711 | Common:1; Rare:82 | ||||
| chr5:55307620-55308106 | Common:5; Rare:181 | ||||
| chr5:55534638-55534774 | Common:2; Rare:49 | ||||
| chr5:55534948-55535179 | Common:1; Rare:79 | ||||
| chr5:55994807-55995148 | Rare:114 | ||||
| chr5:56815254-56815571 | Common:3; Rare:117 | ||||
| chr5:56909376-56909637 | Common:3; Rare:67 | ||||
| chr5:56952098-56952382 | Rare:108 |