| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:49788875-49789429 | Common:3; Rare:150 | ||||
| chr17:49848039-49848382 | Rare:75 | ||||
| chr17:49968397-49968843 | Common:2; Rare:93 | ||||
| chr17:49968934-49969214 | Common:2; Rare:56 | ||||
| chr17:49969448-49969525 | Rare:28 | ||||
| chr17:49993442-49993473 | Rare:7; Clinvar:1 | ||||
| chr17:49993531-49993593 | Rare:18 | ||||
| chr17:49995197-49995328 | Rare:25; Clinvar:1 | ||||
| chr17:50055672-50056207 | Common:6; Rare:120 | ||||
| chr17:50095132-50095391 | Common:1; Rare:79 | ||||
| chr17:50149924-50150137 | Common:10; Rare:68; Clinvar:4 | ||||
| chr17:50150305-50150366 | Rare:8 | ||||
| chr17:50151044-50151297 | Common:1; Rare:58 | ||||
| chr17:50199752-50200009 | Common:1; Rare:85; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr17:50200200-50200338 | Common:1; Rare:26 |