| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:34008027-34008214 | Common:2; Rare:69; Clinvar:2; Clinvar (benign):1 | ||||
| chr5:34656144-34656497 | Common:3; Rare:90 | ||||
| chr5:34839270-34839396 | Common:2; Rare:39 | ||||
| chr5:34915483-34915741 | Common:1; Rare:62 | ||||
| chr5:34929512-34930021 | Common:1; Rare:173 | ||||
| chr5:35230339-35230478 | Common:1; Rare:27 | ||||
| chr5:35617721-35617928 | Common:1; Rare:40 | ||||
| chr5:36151812-36152187 | Rare:107 | ||||
| chr5:36606456-36606716 | Rare:47 | ||||
| chr5:36876625-36876915 | Common:1; Rare:86; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:36877096-36877155 | Rare:27; Clinvar:1 | ||||
| chr5:37248991-37249055 | Common:1; Rare:12 | ||||
| chr5:37371040-37371184 | Rare:50 | ||||
| chr5:37379059-37379364 | Common:3; Rare:72 | ||||
| chr5:38258418-38258580 | Common:1; Rare:42 |