| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:126595169-126595361 | Common:4; Rare:87; Clinvar:5; Clinvar (benign):9 | ||||
| chr5:126776879-126777175 | Common:2; Rare:119; Clinvar:4; Clinvar (benign):4 | ||||
| chr5:127030491-127030678 | Common:2; Rare:49 | ||||
| chr5:127290654-127290844 | Rare:42 | ||||
| chr5:127517504-127517776 | Common:6; Rare:115 | ||||
| chr5:128083230-128083345 | Rare:39 | ||||
| chr5:128083551-128083766 | Common:2; Rare:88 | ||||
| chr5:128538238-128538434 | Common:4; Rare:63 | ||||
| chr5:129094470-129094787 | Common:3; Rare:137 | ||||
| chr5:131165190-131165373 | Common:1; Rare:72; Clinvar (benign):1 | ||||
| chr5:131170692-131171013 | Common:1; Rare:68; Clinvar (benign):2 | ||||
| chr5:131263910-131264139 | Rare:87 | ||||
| chr5:131635153-131635432 | Common:1; Rare:107 | ||||
| chr5:131796910-131797215 | Rare:88 | ||||
| chr5:132257475-132257727 | Common:8; Rare:65 |