| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:16465723-16465895 | Rare:30 | ||||
| chr5:31532043-31532352 | Common:3; Rare:87 | ||||
| chr5:32174267-32174428 | Common:2; Rare:57 | ||||
| chr5:32531709-32531867 | Common:1; Rare:31 | ||||
| chr5:33440632-33441058 | Common:6; Rare:113 | ||||
| chr5:34008027-34008196 | Common:2; Rare:63; Clinvar:2; Clinvar (benign):1 | ||||
| chr5:34915212-34915317 | Rare:29 | ||||
| chr5:34915472-34915741 | Common:1; Rare:65 | ||||
| chr5:36151885-36152180 | Rare:93 | ||||
| chr5:36876650-36876859 | Common:1; Rare:63; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:37371053-37371439 | Common:2; Rare:95 | ||||
| chr5:37379184-37379364 | Rare:47 | ||||
| chr5:39074373-39074539 | Common:1; Rare:76 | ||||
| chr5:40755907-40756040 | Rare:39 | ||||
| chr5:40798148-40798448 | Common:1; Rare:117 |