| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:43041427-43041742 | Common:4; Rare:53 | ||||
| chr5:43065760-43066067 | Common:3; Rare:47 | ||||
| chr5:43066943-43067040 | Rare:30 | ||||
| chr5:52922397-52922699 | Common:1; Rare:45 | ||||
| chr5:53101430-53101713 | Common:4; Rare:80; Clinvar:2; Clinvar (benign):1 | ||||
| chr5:53485002-53485435 | Common:1; Rare:91 | ||||
| chr5:54148564-54148662 | Rare:11 | ||||
| chr5:55372977-55373033 | Rare:11 | ||||
| chr5:55431163-55431316 | Rare:25 | ||||
| chr5:55431926-55432072 | Rare:35 | ||||
| chr5:57488366-57488651 | Common:2; Rare:41 | ||||
| chr5:61152042-61152261 | Common:1; Rare:38 | ||||
| chr5:61337562-61337829 | Rare:47 | ||||
| chr5:61391896-61392102 | Rare:39 | ||||
| chr5:64750921-64751028 | Rare:26 |