| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:45432833-45432984 | Rare:32 | ||||
| chr17:45490691-45490950 | Common:7; Rare:83 | ||||
| chr17:45620163-45620262 | Rare:21 | ||||
| chr17:46192810-46193028 | Common:2; Rare:54; Clinvar (benign):1 | ||||
| chr17:46193396-46193742 | Common:4; Rare:97 | ||||
| chr17:46193943-46194270 | Common:5; Rare:53 | ||||
| chr17:46225409-46225547 | Common:3; Rare:39 | ||||
| chr17:46922782-46923246 | Common:5; Rare:147; Clinvar:5; Clinvar (benign):12; Clinvar (pathogenic):1 | ||||
| chr17:47188843-47188851 | |||||
| chr17:47188996-47189065 | Rare:19 | ||||
| chr17:47189101-47189136 | Rare:11 | ||||
| chr17:47189208-47189631 | Common:1; Rare:115 | ||||
| chr17:47200165-47200284 | Rare:12 | ||||
| chr17:47253656-47253843 | Common:2; Rare:46 | ||||
| chr17:47253880-47253990 | Common:1; Rare:35; Clinvar:1; Clinvar (benign):3 |