| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:50150966-50151407 | Common:2; Rare:217 | ||||
| chr17:50199650-50200120 | Common:6; Rare:205; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr17:50200211-50200550 | Common:4; Rare:64; Clinvar:1 | ||||
| chr17:50345834-50346226 | Common:14; Rare:306 | ||||
| chr17:50372863-50373298 | Common:12; Rare:328 | ||||
| chr17:50384136-50385538 | Common:13; Rare:429 | ||||
| chr17:50397420-50397717 | Common:5; Rare:148 | ||||
| chr17:50425999-50426307 | Common:6; Rare:218 | ||||
| chr17:50478645-50479117 | Common:8; Rare:245 | ||||
| chr17:50508340-50508770 | Common:3; Rare:145 | ||||
| chr17:50532428-50532821 | Common:10; Rare:187 | ||||
| chr17:50534310-50534615 | Common:3; Rare:183 | ||||
| chr17:50547173-50547844 | Common:3; Rare:345 | ||||
| chr17:50634665-50634962 | Common:3; Rare:81 | ||||
| chr17:50661900-50662242 | Common:1; Rare:68 |