| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:48908295-48908512 | Common:1; Rare:56 | ||||
| chr17:48944773-48944924 | Common:2; Rare:50 | ||||
| chr17:49132441-49132805 | Common:4; Rare:66 | ||||
| chr17:49210572-49210720 | Rare:21 | ||||
| chr17:49707865-49707965 | Rare:56 | ||||
| chr17:49708104-49708327 | Common:1; Rare:77 | ||||
| chr17:49788557-49788759 | Common:1; Rare:69 | ||||
| chr17:50055762-50056127 | Common:4; Rare:82 | ||||
| chr17:50095064-50095427 | Common:2; Rare:114 | ||||
| chr17:50105649-50105976 | Common:3; Rare:74 | ||||
| chr17:50188901-50189172 | Rare:72; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr17:50271436-50271489 | Rare:7 | ||||
| chr17:50274354-50274547 | Common:2; Rare:57 | ||||
| chr17:50274661-50274956 | Rare:53 | ||||
| chr17:50373158-50373254 | Common:3; Rare:43 |