| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:44345007-44345334 | Rare:72; Clinvar:5; Clinvar (benign):4 | ||||
| chr17:44503344-44503730 | Rare:146 | ||||
| chr17:44708516-44708899 | Common:4; Rare:101 | ||||
| chr17:44829589-44829715 | Common:1; Rare:38 | ||||
| chr17:44847567-44847921 | Common:1; Rare:65 | ||||
| chr17:44899367-44899735 | Common:2; Rare:114; Clinvar:1; Clinvar (benign):1 | ||||
| chr17:44911509-44911592 | Common:3; Rare:25; Clinvar:2 | ||||
| chr17:45051453-45051691 | Common:1; Rare:84 | ||||
| chr17:45060987-45061339 | Common:2; Rare:93 | ||||
| chr17:45132538-45132635 | Rare:37 | ||||
| chr17:45148142-45148478 | Common:1; Rare:94 | ||||
| chr17:45161494-45161902 | Common:1; Rare:109 | ||||
| chr17:45490713-45490887 | Rare:58 | ||||
| chr17:45894278-45894570 | Common:2; Rare:86; Clinvar:4; Clinvar (benign):1 | ||||
| chr17:46193406-46193604 | Common:3; Rare:53 |