| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:140116485-140116638 | Common:1; Rare:26 | ||||
| chr5:140121940-140122216 | Rare:43 | ||||
| chr5:140128376-140128537 | Common:1; Rare:38 | ||||
| chr5:140390794-140390861 | Rare:3 | ||||
| chr5:140527988-140528146 | Rare:38 | ||||
| chr5:140556266-140556338 | Rare:15 | ||||
| chr5:140676987-140677420 | Common:1; Rare:94; Clinvar:5 | ||||
| chr5:140703617-140703991 | Rare:67 | ||||
| chr5:141318547-141319299 | Common:2; Rare:166 | ||||
| chr5:141319409-141319964 | Common:2; Rare:110 | ||||
| chr5:141477785-141478103 | Rare:88 | ||||
| chr5:141528471-141528860 | Rare:102; Clinvar:4; Clinvar (benign):6 | ||||
| chr5:141528863-141529268 | Rare:100; Clinvar:2; Clinvar (benign):1 | ||||
| chr5:141580476-141580874 | Rare:91; Clinvar:3; Clinvar (benign):1 | ||||
| chr5:141583257-141583642 | Rare:79 |