| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:27471874-27472029 | Rare:26 | ||||
| chr17:28041653-28041743 | Common:1; Rare:20 | ||||
| chr17:28042827-28043016 | Rare:55 | ||||
| chr17:28318918-28319327 | Common:3; Rare:146 | ||||
| chr17:28331968-28332266 | Common:1; Rare:73 | ||||
| chr17:28335356-28335824 | Common:1; Rare:111 | ||||
| chr17:28357312-28357699 | Common:11; Rare:179; Clinvar (pathogenic):1 | ||||
| chr17:28370239-28370348 | Rare:14 | ||||
| chr17:28371371-28371722 | Common:5; Rare:64 | ||||
| chr17:28552514-28552691 | Rare:73; Clinvar:3; Clinvar (benign):1 | ||||
| chr17:28571462-28571716 | Rare:76 | ||||
| chr17:28576875-28577011 | Common:1; Rare:39 | ||||
| chr17:28598935-28599184 | Common:3; Rare:80 | ||||
| chr17:28633097-28633249 | Rare:37 | ||||
| chr17:28645078-28645338 | Common:1; Rare:103 |