| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:52787605-52788057 | Common:1; Rare:103 | ||||
| chr5:52788122-52788263 | Common:1; Rare:36 | ||||
| chr5:52865035-52865360 | Common:1; Rare:71 | ||||
| chr5:52989187-52989421 | Common:4; Rare:64; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:53109716-53109915 | Common:1; Rare:103; Clinvar:3 | ||||
| chr5:53480313-53480409 | Rare:14 | ||||
| chr5:53482559-53483070 | Common:2; Rare:108 | ||||
| chr5:53483143-53483446 | Rare:49 | ||||
| chr5:53484070-53484473 | Common:1; Rare:93 | ||||
| chr5:53560595-53560755 | Common:1; Rare:76; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr5:55160090-55160397 | Rare:91 | ||||
| chr5:55307394-55307824 | Common:3; Rare:164 | ||||
| chr5:55307897-55308147 | Common:2; Rare:106 | ||||
| chr5:55982770-55982897 | Rare:19 | ||||
| chr5:55994773-55995206 | Common:1; Rare:152 |