| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:75784550-75784906 | Common:4; Rare:324 | ||||
| chr17:75784962-75785203 | Common:7; Rare:68 | ||||
| chr17:75844056-75844296 | Common:3; Rare:114; Clinvar:2; Clinvar (benign):4 | ||||
| chr17:75844327-75844453 | Rare:64; Clinvar:1 | ||||
| chr17:75844481-75844893 | Common:9; Rare:147; Clinvar:14; Clinvar (benign):5 | ||||
| chr17:75855257-75855728 | Common:4; Rare:248 | ||||
| chr17:75877140-75877555 | Common:4; Rare:129 | ||||
| chr17:75878545-75878738 | Common:6; Rare:133 | ||||
| chr17:75896250-75896650 | Common:7; Rare:154 | ||||
| chr17:75896776-75897059 | Common:2; Rare:141 | ||||
| chr17:75904821-75905229 | Common:10; Rare:211 | ||||
| chr17:75940888-75941260 | Common:3; Rare:169 | ||||
| chr17:75979084-75979290 | Rare:110; Clinvar:8 | ||||
| chr17:75979387-75979629 | Common:1; Rare:142; Clinvar (benign):1 | ||||
| chr17:76027206-76027578 | Rare:146 |