| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:75717381-75717663 | Common:5; Rare:70 | ||||
| chr5:77030289-77030421 | Rare:44 | ||||
| chr5:77492174-77492259 | Rare:33 | ||||
| chr5:78360355-78360698 | Common:5; Rare:131 | ||||
| chr5:79069627-79069777 | Rare:52; Clinvar (benign):2 | ||||
| chr5:79235900-79236132 | Common:4; Rare:98 | ||||
| chr5:79612289-79612615 | Rare:89 | ||||
| chr5:79991208-79991356 | Rare:45 | ||||
| chr5:80255894-80256244 | Common:3; Rare:139 | ||||
| chr5:80407874-80408103 | Common:1; Rare:83 | ||||
| chr5:80487897-80488124 | Common:1; Rare:73 | ||||
| chr5:80654368-80654738 | Common:5; Rare:178 | ||||
| chr5:81301490-81301698 | Common:4; Rare:73 | ||||
| chr5:81751019-81751372 | Common:1; Rare:97 | ||||
| chr5:82278319-82278670 | Common:3; Rare:111 |