| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:124748777-124748915 | Common:2; Rare:25 | ||||
| chr5:126423320-126423560 | Rare:62 | ||||
| chr5:126595147-126595304 | Common:2; Rare:78; Clinvar:5; Clinvar (benign):7; Clinvar (pathogenic):3 | ||||
| chr5:126600711-126601042 | Common:1; Rare:120 | ||||
| chr5:127030511-127030755 | Common:2; Rare:58 | ||||
| chr5:127031248-127031369 | Rare:20 | ||||
| chr5:127073445-127073554 | Common:3; Rare:36 | ||||
| chr5:127290756-127290852 | Rare:16 | ||||
| chr5:127517495-127517756 | Common:7; Rare:109 | ||||
| chr5:128084006-128084362 | Common:4; Rare:112 | ||||
| chr5:128339157-128339267 | Rare:18 | ||||
| chr5:128965413-128965566 | Common:2; Rare:46 | ||||
| chr5:129094514-129094779 | Common:2; Rare:115 | ||||
| chr5:129903698-129904067 | Rare:74 | ||||
| chr5:131165190-131165391 | Common:2; Rare:82; Clinvar (benign):1 |