| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:31532037-31532352 | Common:3; Rare:88 | ||||
| chr5:32174218-32174427 | Common:2; Rare:77 | ||||
| chr5:32709968-32710536 | Common:4; Rare:101 | ||||
| chr5:32710561-32710768 | Common:1; Rare:50 | ||||
| chr5:32712217-32712284 | Rare:13 | ||||
| chr5:33440593-33441116 | Common:7; Rare:146 | ||||
| chr5:33461009-33461227 | Common:3; Rare:61 | ||||
| chr5:34008020-34008214 | Common:2; Rare:71; Clinvar:2; Clinvar (benign):1 | ||||
| chr5:34656150-34656547 | Common:3; Rare:97 | ||||
| chr5:34839254-34839419 | Common:2; Rare:51 | ||||
| chr5:34915212-34915313 | Rare:29 | ||||
| chr5:34915453-34915766 | Common:1; Rare:88 | ||||
| chr5:34929687-34930029 | Common:1; Rare:106 | ||||
| chr5:35856693-35857002 | Rare:62 | ||||
| chr5:36151803-36152177 | Rare:101 |