| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:44324754-44324987 | Common:2; Rare:85 | ||||
| chr17:44503349-44503720 | Rare:141 | ||||
| chr17:44656253-44656515 | Common:6; Rare:99 | ||||
| chr17:44708537-44708948 | Common:4; Rare:107 | ||||
| chr17:44899359-44899799 | Common:3; Rare:132; Clinvar:3; Clinvar (benign):1 | ||||
| chr17:44947741-44947880 | Common:1; Rare:40 | ||||
| chr17:45051443-45051699 | Common:1; Rare:89 | ||||
| chr17:45060783-45060949 | Rare:33 | ||||
| chr17:45060958-45061399 | Common:3; Rare:127 | ||||
| chr17:45061505-45061705 | Rare:44 | ||||
| chr17:45132288-45132631 | Common:2; Rare:105 | ||||
| chr17:45148150-45148631 | Common:1; Rare:163 | ||||
| chr17:45148892-45149193 | Common:4; Rare:84 | ||||
| chr17:45160792-45161143 | Common:1; Rare:106 | ||||
| chr17:45161265-45161281 | Rare:5 |