| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:49994673-49994786 | Rare:37; Clinvar:1 | ||||
| chr17:50055735-50056136 | Common:5; Rare:87 | ||||
| chr17:50056137-50056604 | Common:1; Rare:117 | ||||
| chr17:50063844-50064174 | Common:1; Rare:52 | ||||
| chr17:50095067-50095494 | Common:2; Rare:134 | ||||
| chr17:50165731-50166033 | Common:1; Rare:68; Clinvar:2; Clinvar (benign):2 | ||||
| chr17:50345895-50346161 | Common:4; Rare:93 | ||||
| chr17:50373160-50373220 | Common:2; Rare:28 | ||||
| chr17:50468863-50468953 | Common:1; Rare:27 | ||||
| chr17:50534392-50534645 | Common:2; Rare:66 | ||||
| chr17:50707972-50708031 | Rare:13 | ||||
| chr17:50719456-50719792 | Rare:119 | ||||
| chr17:50866271-50866774 | Common:4; Rare:148 | ||||
| chr17:51166273-51166955 | Common:4; Rare:180 | ||||
| chr17:51260128-51260813 | Common:4; Rare:287 |