| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:119268596-119268811 | Common:1; Rare:62 | ||||
| chr5:119355825-119356021 | Common:2; Rare:50 | ||||
| chr5:122311526-122311774 | Common:3; Rare:44 | ||||
| chr5:122845503-122845621 | Common:3; Rare:45 | ||||
| chr5:123036452-123036536 | Rare:39 | ||||
| chr5:123036552-123036851 | Common:2; Rare:80 | ||||
| chr5:124748753-124749004 | Common:2; Rare:55 | ||||
| chr5:126423324-126423613 | Rare:82 | ||||
| chr5:126600847-126601054 | Common:1; Rare:96 | ||||
| chr5:127030509-127030768 | Common:2; Rare:62 | ||||
| chr5:127517490-127517754 | Common:7; Rare:112 | ||||
| chr5:128965192-128965561 | Common:4; Rare:99 | ||||
| chr5:131165153-131165392 | Common:2; Rare:96; Clinvar (benign):1 | ||||
| chr5:131635153-131635422 | Common:1; Rare:101 | ||||
| chr5:131796936-131797202 | Rare:79 |