| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:115296561-115296896 | Common:3; Rare:45 | ||||
| chr5:115544639-115545005 | Common:2; Rare:133 | ||||
| chr5:115841490-115842065 | Common:8; Rare:250 | ||||
| chr5:116084780-116085067 | Common:8; Rare:107 | ||||
| chr5:116085359-116085462 | Rare:25 | ||||
| chr5:119268573-119268837 | Common:1; Rare:72 | ||||
| chr5:121961891-121962045 | Common:2; Rare:62 | ||||
| chr5:122077107-122077257 | Common:1; Rare:25 | ||||
| chr5:122774859-122775115 | Common:1; Rare:96 | ||||
| chr5:122845516-122845621 | Common:3; Rare:40 | ||||
| chr5:123036651-123036781 | Common:1; Rare:38 | ||||
| chr5:123511975-123512268 | Common:1; Rare:81 | ||||
| chr5:126423292-126423479 | Rare:45 | ||||
| chr5:126595127-126595370 | Common:5; Rare:110; Clinvar:7; Clinvar (benign):11; Clinvar (pathogenic):3 | ||||
| chr5:126776931-126777175 | Common:1; Rare:95; Clinvar:3; Clinvar (benign):1 |