| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:50441176-50441241 | Rare:17 | ||||
| chr5:50666822-50666967 | Common:1; Rare:37 | ||||
| chr5:50667298-50667425 | Common:1; Rare:45 | ||||
| chr5:50667755-50668054 | Common:1; Rare:90 | ||||
| chr5:52787584-52788031 | Common:6; Rare:99 | ||||
| chr5:53109729-53109926 | Common:1; Rare:95; Clinvar:2 | ||||
| chr5:53480220-53480789 | Common:2; Rare:154 | ||||
| chr5:53483143-53483176 | Rare:4 | ||||
| chr5:53560478-53560755 | Common:1; Rare:99; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr5:54310507-54310729 | Common:1; Rare:75 | ||||
| chr5:55307604-55307893 | Common:3; Rare:97 | ||||
| chr5:55307903-55308147 | Common:2; Rare:104 | ||||
| chr5:55534591-55534768 | Common:2; Rare:62 | ||||
| chr5:55534949-55535179 | Common:1; Rare:79 | ||||
| chr5:55994925-55995206 | Rare:107 |