| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:75042527-75042960 | Common:3; Rare:89 | ||||
| chr17:75046929-75047194 | Common:1; Rare:81 | ||||
| chr17:75109878-75109975 | Common:1; Rare:23 | ||||
| chr17:75130753-75131093 | Common:2; Rare:118 | ||||
| chr17:75205399-75205749 | Rare:109 | ||||
| chr17:75261577-75261925 | Common:4; Rare:105; Clinvar (benign):1 | ||||
| chr17:75271142-75271390 | Common:3; Rare:45 | ||||
| chr17:75289420-75289630 | Rare:61; Clinvar:1 | ||||
| chr17:75456433-75456662 | Common:1; Rare:67 | ||||
| chr17:75515437-75515681 | Common:3; Rare:76 | ||||
| chr17:75516407-75516570 | Common:1; Rare:49; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr17:75525483-75525765 | Common:2; Rare:93 | ||||
| chr17:75639946-75640161 | Common:1; Rare:51 | ||||
| chr17:75667122-75667474 | Common:5; Rare:118 | ||||
| chr17:75721187-75721611 | Common:3; Rare:128; Clinvar:3 |