| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:41925087-41925305 | Common:1; Rare:82 | ||||
| chr5:43121360-43121602 | Common:1; Rare:89 | ||||
| chr5:43603086-43603219 | Rare:34 | ||||
| chr5:50441108-50441125 | Rare:11 | ||||
| chr5:50666773-50667150 | Common:1; Rare:106 | ||||
| chr5:50667280-50667421 | Common:1; Rare:47 | ||||
| chr5:50667760-50667912 | Common:1; Rare:49 | ||||
| chr5:55307654-55308035 | Common:5; Rare:131 | ||||
| chr5:56815218-56815334 | Common:1; Rare:43 | ||||
| chr5:57173537-57173922 | Common:3; Rare:141 | ||||
| chr5:58491357-58491539 | Common:2; Rare:33 | ||||
| chr5:60944992-60945238 | Common:5; Rare:101; Clinvar:4; Clinvar (benign):5 | ||||
| chr5:61162377-61162667 | Common:1; Rare:79 | ||||
| chr5:62412490-62412778 | Rare:93 | ||||
| chr5:64768530-64768969 | Common:5; Rare:120 |