| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:119070880-119071009 | Common:1; Rare:35 | ||||
| chr5:119268584-119268821 | Common:1; Rare:68 | ||||
| chr5:119355825-119356019 | Common:2; Rare:50 | ||||
| chr5:119452364-119452549 | Common:1; Rare:63; Clinvar (benign):2 | ||||
| chr5:124748820-124749004 | Common:1; Rare:47 | ||||
| chr5:126776907-126777187 | Common:1; Rare:109; Clinvar:4; Clinvar (benign):3 | ||||
| chr5:127073465-127073554 | Common:3; Rare:29 | ||||
| chr5:127517504-127517716 | Common:6; Rare:95 | ||||
| chr5:131165206-131165357 | Rare:63; Clinvar (benign):1 | ||||
| chr5:131170692-131171011 | Common:1; Rare:68; Clinvar (benign):2 | ||||
| chr5:131252946-131253059 | Common:1; Rare:26 | ||||
| chr5:131635163-131635395 | Common:1; Rare:88 | ||||
| chr5:131635669-131635723 | Rare:12 | ||||
| chr5:131796938-131797192 | Rare:75 | ||||
| chr5:132556813-132557012 | Common:1; Rare:66; Clinvar:1 |