| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:43121406-43121648 | Common:1; Rare:93 | ||||
| chr5:43313393-43313672 | Common:3; Rare:75 | ||||
| chr5:43483837-43483955 | Common:1; Rare:42 | ||||
| chr5:43602572-43602741 | Common:2; Rare:32 | ||||
| chr5:43602852-43603288 | Rare:103 | ||||
| chr5:44808716-44808976 | Common:2; Rare:87 | ||||
| chr5:50667312-50667399 | Rare:33 | ||||
| chr5:53109716-53109909 | Common:1; Rare:98; Clinvar:3 | ||||
| chr5:53560315-53560755 | Common:2; Rare:118; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr5:54310513-54310711 | Rare:63 | ||||
| chr5:54455492-54456009 | Common:2; Rare:142; Clinvar:4; Clinvar (benign):4 | ||||
| chr5:55307639-55308049 | Common:5; Rare:145 | ||||
| chr5:55534611-55534768 | Common:2; Rare:55 | ||||
| chr5:55534949-55535205 | Common:1; Rare:86 | ||||
| chr5:57173540-57174132 | Common:3; Rare:207 |