| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:50195256-50195473 | Rare:66; Clinvar:1; Clinvar (benign):4 | ||||
| chr17:50373118-50373231 | Common:2; Rare:55 | ||||
| chr17:51166695-51166954 | Rare:78 | ||||
| chr17:54968608-54968795 | Common:3; Rare:91 | ||||
| chr17:56914007-56914140 | Common:1; Rare:35 | ||||
| chr17:58007216-58007396 | Common:1; Rare:78 | ||||
| chr17:59106838-59107124 | Common:1; Rare:103; Clinvar:2; Clinvar (benign):1 | ||||
| chr17:59155153-59155426 | Common:2; Rare:69 | ||||
| chr17:59155445-59155781 | Rare:86 | ||||
| chr17:59619561-59619962 | Common:3; Rare:143 | ||||
| chr17:59707380-59707742 | Common:4; Rare:100; Clinvar (benign):6 | ||||
| chr17:59892856-59893136 | Rare:81 | ||||
| chr17:60525930-60526311 | Common:2; Rare:129 | ||||
| chr17:61399514-61399928 | Common:1; Rare:113 | ||||
| chr17:62627247-62627423 | Rare:39 |