| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:43121419-43121655 | Common:1; Rare:88 | ||||
| chr5:43396831-43397006 | Common:1; Rare:43 | ||||
| chr5:43483837-43483913 | Common:1; Rare:31 | ||||
| chr5:43515060-43515243 | Common:3; Rare:68 | ||||
| chr5:43602886-43603204 | Rare:79 | ||||
| chr5:44808674-44809043 | Common:2; Rare:134 | ||||
| chr5:50441214-50441431 | Common:3; Rare:61 | ||||
| chr5:50667156-50667425 | Common:1; Rare:89 | ||||
| chr5:50667755-50667957 | Common:1; Rare:64 | ||||
| chr5:52989066-52989365 | Common:5; Rare:84; Clinvar (benign):1 | ||||
| chr5:53109716-53109901 | Common:1; Rare:95; Clinvar:3 | ||||
| chr5:54310507-54310714 | Rare:67 | ||||
| chr5:55160125-55160224 | Rare:30 | ||||
| chr5:55307620-55308043 | Common:5; Rare:149 | ||||
| chr5:56909378-56909638 | Common:3; Rare:67 |