| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:50056036-50056182 | Common:1; Rare:41 | ||||
| chr17:50056717-50056936 | Common:1; Rare:35 | ||||
| chr17:50373160-50373253 | Common:3; Rare:41 | ||||
| chr17:50719430-50719647 | Common:1; Rare:88 | ||||
| chr17:50866312-50866514 | Common:3; Rare:76 | ||||
| chr17:51260368-51260617 | Common:3; Rare:122 | ||||
| chr17:54968599-54968792 | Common:3; Rare:91 | ||||
| chr17:55751263-55751426 | Common:2; Rare:65 | ||||
| chr17:56913472-56913561 | Rare:30 | ||||
| chr17:56913980-56914180 | Common:1; Rare:55 | ||||
| chr17:57084960-57085359 | Common:1; Rare:129 | ||||
| chr17:57849995-57850274 | Common:1; Rare:92 | ||||
| chr17:57988147-57988524 | Common:5; Rare:110 | ||||
| chr17:58007216-58007384 | Common:1; Rare:72 | ||||
| chr17:58219216-58219342 | Common:1; Rare:47; Clinvar:2; Clinvar (benign):4 |