| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:75289369-75289656 | Common:5; Rare:168; Clinvar:2; Clinvar (benign):4 | ||||
| chr17:75393670-75394064 | Common:2; Rare:178 | ||||
| chr17:75456401-75456733 | Common:2; Rare:196 | ||||
| chr17:75515432-75515738 | Common:6; Rare:176 | ||||
| chr17:75516361-75516602 | Common:4; Rare:124; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr17:75525407-75525818 | Common:6; Rare:211 | ||||
| chr17:75557571-75557886 | Common:4; Rare:124 | ||||
| chr17:75646030-75646354 | Common:5; Rare:104 | ||||
| chr17:75667107-75667418 | Common:8; Rare:211 | ||||
| chr17:75753690-75754807 | Common:4; Rare:338; Clinvar:7; Clinvar (benign):1 | ||||
| chr17:75764040-75764360 | Common:1; Rare:146; Clinvar:1; Clinvar (benign):1 | ||||
| chr17:75765144-75765333 | Common:2; Rare:56; Clinvar:1 | ||||
| chr17:75784555-75784905 | Common:4; Rare:306 | ||||
| chr17:75844029-75844323 | Common:2; Rare:121; Clinvar:3; Clinvar (benign):3 | ||||
| chr17:75855283-75855749 | Common:4; Rare:245 |