| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:45148165-45148478 | Common:1; Rare:93 | ||||
| chr17:45490708-45490867 | Rare:55 | ||||
| chr17:46192847-46193019 | Common:1; Rare:44 | ||||
| chr17:46193345-46193604 | Common:4; Rare:72 | ||||
| chr17:47188845-47189036 | Common:1; Rare:38 | ||||
| chr17:47189202-47189351 | Common:1; Rare:46 | ||||
| chr17:47323890-47323992 | Common:1; Rare:28 | ||||
| chr17:47591786-47592008 | Common:1; Rare:55 | ||||
| chr17:47649534-47649786 | Common:1; Rare:70 | ||||
| chr17:47649952-47650274 | Rare:99 | ||||
| chr17:47941356-47941712 | Rare:97; Clinvar:5; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr17:48048057-48048405 | Rare:93 | ||||
| chr17:48048643-48048872 | Common:3; Rare:38 | ||||
| chr17:48107465-48107784 | Common:5; Rare:74 | ||||
| chr17:48544562-48544590 | Rare:12 |