| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:44324721-44324989 | Common:4; Rare:98 | ||||
| chr17:44325209-44325403 | Common:2; Rare:41 | ||||
| chr17:44352016-44352588 | Common:1; Rare:186; Clinvar:16; Clinvar (benign):6; Clinvar (pathogenic):3 | ||||
| chr17:44503332-44503714 | Rare:144 | ||||
| chr17:44557055-44557349 | Common:1; Rare:55 | ||||
| chr17:44899369-44899769 | Common:3; Rare:126; Clinvar:3; Clinvar (benign):1 | ||||
| chr17:45051437-45051688 | Common:1; Rare:86 | ||||
| chr17:45060964-45061411 | Common:2; Rare:134 | ||||
| chr17:45104754-45104984 | Rare:40 | ||||
| chr17:45105386-45105661 | Common:3; Rare:65 | ||||
| chr17:45132288-45132657 | Common:3; Rare:113 | ||||
| chr17:45148147-45148615 | Common:1; Rare:159 | ||||
| chr17:45161489-45161926 | Common:1; Rare:114 | ||||
| chr17:45490708-45490898 | Rare:64 | ||||
| chr17:45620244-45620366 | Rare:30 |