| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:122845308-122845654 | Common:3; Rare:123 | ||||
| chr5:123036288-123036487 | Common:1; Rare:58 | ||||
| chr5:123423226-123423609 | Common:1; Rare:117 | ||||
| chr5:123511951-123512280 | Common:1; Rare:99 | ||||
| chr5:123512435-123512560 | Rare:35 | ||||
| chr5:124748804-124749004 | Common:1; Rare:50 | ||||
| chr5:126595126-126595340 | Common:4; Rare:100; Clinvar:7; Clinvar (benign):10; Clinvar (pathogenic):3 | ||||
| chr5:126776857-126777168 | Common:3; Rare:121; Clinvar:4; Clinvar (benign):5 | ||||
| chr5:127030539-127030764 | Common:2; Rare:52 | ||||
| chr5:128082832-128083476 | Common:8; Rare:196 | ||||
| chr5:128083895-128084147 | Common:1; Rare:58 | ||||
| chr5:128538188-128538372 | Common:5; Rare:62 | ||||
| chr5:131165092-131165382 | Common:3; Rare:107; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr5:131170693-131171008 | Common:1; Rare:67; Clinvar (benign):2 | ||||
| chr5:131263626-131264163 | Common:2; Rare:174 |