| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:75456442-75456737 | Common:1; Rare:92 | ||||
| chr17:75515423-75515652 | Common:3; Rare:67 | ||||
| chr17:75522131-75522545 | Common:3; Rare:154; Clinvar:10; Clinvar (benign):3; Clinvar (pathogenic):4 | ||||
| chr17:75524728-75525092 | Common:2; Rare:91; Clinvar (benign):1 | ||||
| chr17:75525424-75525816 | Common:4; Rare:118 | ||||
| chr17:75667100-75667474 | Common:5; Rare:127 | ||||
| chr17:75765141-75765283 | Common:1; Rare:43; Clinvar:1 | ||||
| chr17:75765317-75765455 | Common:1; Rare:32 | ||||
| chr17:75830465-75830626 | Common:1; Rare:66; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr17:75833270-75833363 | Rare:14 | ||||
| chr17:75855295-75855666 | Common:1; Rare:100 | ||||
| chr17:75896731-75896773 | Rare:11 | ||||
| chr17:75905051-75905302 | Common:2; Rare:54 | ||||
| chr17:75940980-75941233 | Common:1; Rare:84 | ||||
| chr17:75979085-75979315 | Rare:63; Clinvar:4 |