| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:48544726-48544750 | Common:1; Rare:9 | ||||
| chr17:48908295-48908506 | Common:1; Rare:55 | ||||
| chr17:48944758-48944886 | Common:1; Rare:47 | ||||
| chr17:49210168-49210436 | Common:2; Rare:41 | ||||
| chr17:49210523-49210718 | Rare:32 | ||||
| chr17:49362136-49362395 | Common:3; Rare:98 | ||||
| chr17:49414834-49415120 | Common:1; Rare:68 | ||||
| chr17:49707861-49707971 | Rare:59 | ||||
| chr17:49788576-49788782 | Common:1; Rare:68 | ||||
| chr17:50055697-50056196 | Common:6; Rare:112 | ||||
| chr17:50056238-50056645 | Common:1; Rare:102 | ||||
| chr17:50063793-50064200 | Common:1; Rare:66 | ||||
| chr17:50095163-50095411 | Common:1; Rare:77 | ||||
| chr17:50188901-50189258 | Rare:90; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr17:50274436-50274504 | Rare:21 |