| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:28406210-28406274 | Rare:9 | ||||
| chr17:28552534-28552726 | Rare:77; Clinvar:3; Clinvar (benign):1 | ||||
| chr17:28571500-28571745 | Rare:63 | ||||
| chr17:28576829-28577054 | Common:2; Rare:58 | ||||
| chr17:28598994-28599170 | Common:2; Rare:49 | ||||
| chr17:28645084-28645314 | Common:1; Rare:87 | ||||
| chr17:28661877-28661976 | Rare:40 | ||||
| chr17:28662102-28662319 | Rare:87 | ||||
| chr17:28717782-28717946 | Rare:35 | ||||
| chr17:28728726-28728824 | Rare:36; Clinvar (benign):1 | ||||
| chr17:28812383-28812641 | Common:1; Rare:67 | ||||
| chr17:28842740-28842873 | Common:1; Rare:49 | ||||
| chr17:28854971-28855034 | Rare:18 | ||||
| chr17:28896810-28897217 | Rare:76 | ||||
| chr17:28897534-28897753 | Common:1; Rare:74 |