| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:122845456-122845621 | Common:3; Rare:61 | ||||
| chr5:123036663-123037018 | Common:2; Rare:89 | ||||
| chr5:124748757-124749051 | Common:3; Rare:65 | ||||
| chr5:126595143-126595336 | Common:4; Rare:90; Clinvar:5; Clinvar (benign):9; Clinvar (pathogenic):3 | ||||
| chr5:126600075-126600249 | Common:1; Rare:31 | ||||
| chr5:126776917-126777220 | Common:2; Rare:114; Clinvar:4; Clinvar (benign):4 | ||||
| chr5:127030511-127030721 | Common:2; Rare:50 | ||||
| chr5:127073471-127073561 | Common:3; Rare:28 | ||||
| chr5:127290676-127290852 | Rare:37 | ||||
| chr5:127517422-127517703 | Common:7; Rare:115 | ||||
| chr5:129094474-129094768 | Common:3; Rare:120 | ||||
| chr5:129460175-129460343 | Common:2; Rare:33 | ||||
| chr5:131165183-131165374 | Common:1; Rare:74; Clinvar (benign):1 | ||||
| chr5:131170670-131171002 | Common:1; Rare:75; Clinvar (benign):1 | ||||
| chr5:131635172-131635374 | Common:1; Rare:76 |