| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:115544728-115545014 | Common:2; Rare:115 | ||||
| chr5:115841490-115841589 | Common:2; Rare:69 | ||||
| chr5:115841831-115842024 | Common:3; Rare:64 | ||||
| chr5:116084965-116085067 | Common:2; Rare:53 | ||||
| chr5:116085403-116085465 | Rare:12 | ||||
| chr5:116574820-116574979 | Common:2; Rare:53 | ||||
| chr5:119070840-119071207 | Common:4; Rare:113 | ||||
| chr5:119071351-119071497 | Rare:67 | ||||
| chr5:119268620-119268835 | Common:1; Rare:59 | ||||
| chr5:119355817-119356021 | Common:2; Rare:52 | ||||
| chr5:119452668-119452785 | Rare:54; Clinvar:2; Clinvar (benign):1 | ||||
| chr5:121961850-121962035 | Common:2; Rare:67 | ||||
| chr5:122774859-122775133 | Common:1; Rare:111 | ||||
| chr5:122845516-122845625 | Common:3; Rare:43 | ||||
| chr5:123036633-123036851 | Common:2; Rare:55 |