| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:28405707-28405984 | Rare:71; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr17:28406139-28406371 | Rare:55; Clinvar:1 | ||||
| chr17:28406546-28406656 | Rare:19 | ||||
| chr17:28552379-28552421 | Rare:11; Clinvar:1 | ||||
| chr17:28552514-28552693 | Rare:74; Clinvar:3; Clinvar (benign):1 | ||||
| chr17:28571453-28571747 | Rare:91 | ||||
| chr17:28576847-28577009 | Common:1; Rare:43 | ||||
| chr17:28598935-28599279 | Common:3; Rare:112 | ||||
| chr17:28599470-28599777 | Rare:58 | ||||
| chr17:28645025-28645420 | Common:1; Rare:165 | ||||
| chr17:28661710-28661770 | Rare:24 | ||||
| chr17:28661836-28661967 | Rare:59 | ||||
| chr17:28662098-28662429 | Rare:106 | ||||
| chr17:28662614-28662638 | Rare:5 | ||||
| chr17:28710931-28711066 | Common:1; Rare:24 |