| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:33440581-33440877 | Common:3; Rare:67 | ||||
| chr5:33440924-33441143 | Common:4; Rare:75 | ||||
| chr5:33441190-33441395 | Common:1; Rare:48 | ||||
| chr5:33891976-33892265 | Rare:62 | ||||
| chr5:34008008-34008267 | Common:2; Rare:100; Clinvar:2; Clinvar (benign):1 | ||||
| chr5:34655839-34656547 | Common:4; Rare:176 | ||||
| chr5:34839319-34839420 | Common:1; Rare:32 | ||||
| chr5:34915212-34915317 | Rare:29 | ||||
| chr5:34915659-34915875 | Common:1; Rare:75 | ||||
| chr5:34929279-34929605 | Common:1; Rare:90 | ||||
| chr5:34929659-34929915 | Rare:84 | ||||
| chr5:35230334-35230425 | Common:1; Rare:19 | ||||
| chr5:35617708-35617902 | Common:1; Rare:33 | ||||
| chr5:35938598-35938811 | Common:1; Rare:40 | ||||
| chr5:35991327-35991485 | Common:1; Rare:28 |