| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:45060958-45061339 | Common:3; Rare:98 | ||||
| chr17:45132369-45132644 | Common:1; Rare:86 | ||||
| chr17:45148142-45148607 | Common:1; Rare:156 | ||||
| chr17:45161027-45161082 | Rare:8 | ||||
| chr17:45161693-45161971 | Common:1; Rare:63 | ||||
| chr17:45490710-45490867 | Rare:54 | ||||
| chr17:46192746-46193003 | Common:3; Rare:60; Clinvar (benign):3 | ||||
| chr17:46193321-46193606 | Common:5; Rare:80 | ||||
| chr17:46579673-46579977 | Rare:29 | ||||
| chr17:46923051-46923190 | Common:2; Rare:56; Clinvar:1; Clinvar (benign):7 | ||||
| chr17:47189135-47189587 | Common:1; Rare:118 | ||||
| chr17:47208740-47208909 | Rare:22 | ||||
| chr17:47208929-47208962 | Rare:5 | ||||
| chr17:47208997-47209578 | Rare:129; Clinvar:2 | ||||
| chr17:47323890-47323992 | Common:1; Rare:28 |