| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:31532043-31532361 | Common:3; Rare:92 | ||||
| chr5:33440605-33441085 | Common:6; Rare:129 | ||||
| chr5:34008027-34008214 | Common:2; Rare:69; Clinvar:2; Clinvar (benign):1 | ||||
| chr5:34656074-34656554 | Common:4; Rare:128 | ||||
| chr5:34915472-34915741 | Common:1; Rare:65 | ||||
| chr5:36151881-36152195 | Rare:100 | ||||
| chr5:39074373-39074544 | Common:1; Rare:81 | ||||
| chr5:39424945-39425322 | Common:3; Rare:76 | ||||
| chr5:40679698-40679975 | Common:1; Rare:63 | ||||
| chr5:40798092-40798401 | Common:1; Rare:114 | ||||
| chr5:40835167-40835432 | Common:3; Rare:105 | ||||
| chr5:41870364-41870556 | Common:1; Rare:63; Clinvar:2; Clinvar (benign):1 | ||||
| chr5:43067409-43067577 | Rare:27 | ||||
| chr5:43121420-43121670 | Common:1; Rare:94 | ||||
| chr5:43483837-43483959 | Common:1; Rare:43 |