| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:75046939-75047116 | Common:1; Rare:52 | ||||
| chr17:75131363-75131663 | Common:1; Rare:95 | ||||
| chr17:75182842-75183222 | Common:2; Rare:130 | ||||
| chr17:75205364-75205751 | Common:1; Rare:126 | ||||
| chr17:75261585-75261980 | Common:4; Rare:136; Clinvar (benign):4 | ||||
| chr17:75270312-75270565 | Common:1; Rare:52 | ||||
| chr17:75271108-75271402 | Common:3; Rare:59 | ||||
| chr17:75393752-75394063 | Common:1; Rare:68 | ||||
| chr17:75456468-75456656 | Rare:50 | ||||
| chr17:75525483-75525739 | Common:2; Rare:83 | ||||
| chr17:75646095-75646354 | Common:4; Rare:57 | ||||
| chr17:75667112-75667386 | Common:4; Rare:93 | ||||
| chr17:75784584-75784905 | Common:2; Rare:146 | ||||
| chr17:75844117-75844224 | Common:2; Rare:34; Clinvar (benign):1 | ||||
| chr17:75844238-75844474 | Rare:73; Clinvar:4; Clinvar (benign):1 |