| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:112737790-112738213 | Rare:92; Clinvar:4; Clinvar (benign):3 | ||||
| chr5:112976453-112976763 | Common:1; Rare:113 | ||||
| chr5:115169705-115170009 | Rare:105 | ||||
| chr5:115180240-115180382 | Common:2; Rare:45 | ||||
| chr5:115544728-115545041 | Common:2; Rare:128 | ||||
| chr5:115816510-115816538 | Rare:4 | ||||
| chr5:115816540-115816596 | Common:1; Rare:17 | ||||
| chr5:115816649-115816867 | Common:1; Rare:58 | ||||
| chr5:115841533-115842069 | Common:7; Rare:221 | ||||
| chr5:116084964-116085055 | Common:2; Rare:44 | ||||
| chr5:116085425-116085482 | Rare:15 | ||||
| chr5:119070867-119071171 | Common:3; Rare:97 | ||||
| chr5:119268604-119268811 | Common:1; Rare:59 | ||||
| chr5:121961695-121962035 | Common:15; Rare:123 | ||||
| chr5:122845267-122845625 | Common:3; Rare:120 |