| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:73498335-73498558 | Common:1; Rare:66 | ||||
| chr5:73565365-73565442 | Rare:15 | ||||
| chr5:73565602-73565820 | Common:5; Rare:94 | ||||
| chr5:74767059-74767361 | Common:2; Rare:95 | ||||
| chr5:75236865-75237086 | Common:5; Rare:82 | ||||
| chr5:75336900-75337277 | Common:3; Rare:131 | ||||
| chr5:75511610-75511921 | Common:1; Rare:113 | ||||
| chr5:75717364-75717663 | Common:5; Rare:75 | ||||
| chr5:77087191-77087307 | Rare:26 | ||||
| chr5:78360355-78360677 | Common:5; Rare:126 | ||||
| chr5:78648509-78648658 | Common:3; Rare:36 | ||||
| chr5:79069633-79069769 | Rare:50; Clinvar (benign):1 | ||||
| chr5:79991227-79991347 | Rare:37 | ||||
| chr5:80255977-80256209 | Common:1; Rare:89 | ||||
| chr5:80407536-80407616 | Rare:17 |