| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:50667280-50667429 | Common:1; Rare:51 | ||||
| chr5:52787823-52787950 | Common:1; Rare:20 | ||||
| chr5:53109711-53109921 | Common:1; Rare:106; Clinvar:4; Clinvar (pathogenic):1 | ||||
| chr5:54310513-54310712 | Rare:64 | ||||
| chr5:55307604-55308015 | Common:4; Rare:144 | ||||
| chr5:55994797-55995199 | Rare:139 | ||||
| chr5:56233261-56233536 | Common:1; Rare:53 | ||||
| chr5:56909490-56909652 | Common:2; Rare:47 | ||||
| chr5:56952109-56952417 | Rare:115 | ||||
| chr5:57173514-57173895 | Common:3; Rare:151 | ||||
| chr5:58460039-58460228 | Common:5; Rare:75 | ||||
| chr5:58581953-58582188 | Common:1; Rare:39 | ||||
| chr5:60488030-60488197 | Common:1; Rare:26 | ||||
| chr5:60700079-60700237 | Common:1; Rare:62 | ||||
| chr5:60844162-60844435 | Common:5; Rare:91 |