| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:50667788-50667932 | Common:1; Rare:47 | ||||
| chr5:51383250-51383448 | Common:2; Rare:73 | ||||
| chr5:52787768-52787957 | Common:1; Rare:39 | ||||
| chr5:53109725-53109890 | Common:1; Rare:83; Clinvar:2 | ||||
| chr5:54310513-54310711 | Rare:63 | ||||
| chr5:55233588-55233882 | Common:4; Rare:102 | ||||
| chr5:55307625-55308029 | Common:5; Rare:139 | ||||
| chr5:55534949-55535198 | Common:1; Rare:84 | ||||
| chr5:55994817-55995184 | Rare:126 | ||||
| chr5:56909476-56909637 | Common:1; Rare:45 | ||||
| chr5:56952104-56952304 | Rare:74 | ||||
| chr5:57173581-57174125 | Common:2; Rare:184 | ||||
| chr5:58460076-58460192 | Common:3; Rare:47 | ||||
| chr5:60844162-60844435 | Common:5; Rare:91 | ||||
| chr5:60945006-60945238 | Common:5; Rare:96; Clinvar:4; Clinvar (benign):5 |