| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:75516360-75516615 | Common:2; Rare:70; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr17:75516873-75517190 | Common:4; Rare:142; Clinvar:3; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
| chr17:75571342-75571441 | Rare:14 | ||||
| chr17:75646154-75646393 | Common:5; Rare:50 | ||||
| chr17:75667116-75667440 | Common:4; Rare:109 | ||||
| chr17:75765056-75765307 | Common:1; Rare:75; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr17:75779434-75779563 | Common:1; Rare:60 | ||||
| chr17:75779728-75780181 | Common:2; Rare:165 | ||||
| chr17:75784550-75784925 | Common:2; Rare:172 | ||||
| chr17:75784951-75785336 | Common:7; Rare:105 | ||||
| chr17:75785863-75785931 | Rare:17 | ||||
| chr17:75785986-75786058 | Rare:16 | ||||
| chr17:75843780-75843869 | Rare:22; Clinvar (pathogenic):1 | ||||
| chr17:75844026-75844213 | Common:2; Rare:50; Clinvar (benign):1 | ||||
| chr17:75844304-75844457 | Rare:42; Clinvar:2; Clinvar (benign):1 |