| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:28570907-28571146 | Rare:79; Clinvar (pathogenic):1 | ||||
| chr17:28571452-28571738 | Rare:89 | ||||
| chr17:28576845-28577078 | Common:2; Rare:61 | ||||
| chr17:28598518-28598588 | Rare:26 | ||||
| chr17:28598728-28598789 | Rare:14 | ||||
| chr17:28598869-28599234 | Common:3; Rare:116 | ||||
| chr17:28599729-28599821 | Rare:20 | ||||
| chr17:28645091-28645483 | Common:1; Rare:137 | ||||
| chr17:28661683-28661804 | Rare:45 | ||||
| chr17:28661837-28661967 | Rare:59 | ||||
| chr17:28662073-28662382 | Rare:102 | ||||
| chr17:28662610-28662719 | Rare:17 | ||||
| chr17:28698283-28698319 | Rare:4 | ||||
| chr17:28698381-28698781 | Common:2; Rare:63 | ||||
| chr17:28710505-28710742 | Common:3; Rare:42 |