| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:75393650-75394160 | Common:6; Rare:497 | ||||
| chr17:75404923-75405158 | Common:2; Rare:111 | ||||
| chr17:75405601-75406038 | Common:5; Rare:266 | ||||
| chr17:75456336-75456736 | Common:8; Rare:460 | ||||
| chr17:75515251-75516118 | Common:22; Rare:774 | ||||
| chr17:75516258-75516662 | Common:14; Rare:365; Clinvar:8; Clinvar (benign):3; Clinvar (pathogenic):5 | ||||
| chr17:75516824-75517318 | Common:16; Rare:491; Clinvar:10; Clinvar (benign):27; Clinvar (pathogenic):3 | ||||
| chr17:75524786-75525186 | Common:4; Rare:222 | ||||
| chr17:75525432-75525832 | Common:14; Rare:482 | ||||
| chr17:75571150-75571590 | Common:3; Rare:104 | ||||
| chr17:75633156-75634150 | Common:5; Rare:347 | ||||
| chr17:75667025-75667472 | Common:30; Rare:690 | ||||
| chr17:75753551-75754073 | Common:6; Rare:425; Clinvar:4 | ||||
| chr17:75754731-75754867 | Common:2; Rare:49; Clinvar:1; Clinvar (benign):1 | ||||
| chr17:75764192-75764311 | Rare:40 |