| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:7224366-7224867 | Common:4; Rare:182; Clinvar:12; Clinvar (benign):22; Clinvar (pathogenic):4 | ||||
| chr17:7234270-7234324 | Rare:24 | ||||
| chr17:7234465-7234667 | Common:2; Rare:107 | ||||
| chr17:7251967-7252750 | Common:4; Rare:293 | ||||
| chr17:7261059-7261202 | Common:1; Rare:37 | ||||
| chr17:7262470-7262648 | Rare:41 | ||||
| chr17:7307246-7307746 | Common:6; Rare:140 | ||||
| chr17:7314292-7314559 | Rare:84 | ||||
| chr17:7315031-7315434 | Common:4; Rare:143 | ||||
| chr17:7352061-7352196 | Rare:44 | ||||
| chr17:7404076-7404245 | Rare:55 | ||||
| chr17:7484215-7484391 | Common:2; Rare:77 | ||||
| chr17:7484602-7484834 | Common:2; Rare:98 | ||||
| chr17:7558202-7558309 | Rare:22 | ||||
| chr17:7576228-7576700 | Common:3; Rare:127 |