| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:112976457-112976847 | Common:3; Rare:173 | ||||
| chr5:113203319-113203549 | Common:6; Rare:54 | ||||
| chr5:113294629-113294672 | Rare:13 | ||||
| chr5:115180206-115180439 | Common:2; Rare:79 | ||||
| chr5:115262813-115262897 | Common:1; Rare:41 | ||||
| chr5:115816393-115816713 | Common:1; Rare:94 | ||||
| chr5:115841331-115841642 | Common:3; Rare:167 | ||||
| chr5:115841873-115842113 | Common:5; Rare:77 | ||||
| chr5:116084919-116085082 | Common:6; Rare:78 | ||||
| chr5:116085407-116085496 | Rare:23 | ||||
| chr5:119070840-119071539 | Common:4; Rare:231 | ||||
| chr5:119268590-119268829 | Common:1; Rare:67 | ||||
| chr5:119452371-119452600 | Common:1; Rare:88; Clinvar:2; Clinvar (benign):4 | ||||
| chr5:119452697-119452785 | Rare:44; Clinvar:2; Clinvar (benign):1 | ||||
| chr5:120465577-120465662 | Common:1; Rare:30 |