| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:4967793-4968106 | Common:1; Rare:98 | ||||
| chr17:4987625-4987753 | Common:1; Rare:52 | ||||
| chr17:5191838-5192113 | Common:2; Rare:88 | ||||
| chr17:5234825-5234946 | Rare:27 | ||||
| chr17:5419634-5419994 | Common:6; Rare:95 | ||||
| chr17:5420091-5420263 | Rare:70 | ||||
| chr17:5486157-5486554 | Common:4; Rare:135 | ||||
| chr17:5486801-5486920 | Common:4; Rare:35 | ||||
| chr17:6640646-6641077 | Common:7; Rare:131 | ||||
| chr17:6651574-6651744 | Common:1; Rare:52 | ||||
| chr17:7012317-7012696 | Rare:129 | ||||
| chr17:7219817-7219956 | Common:3; Rare:65; Clinvar:5; Clinvar (benign):2 | ||||
| chr17:7224008-7224223 | Rare:76; Clinvar:5; Clinvar (benign):4; Clinvar (pathogenic):5 | ||||
| chr17:7241789-7241893 | Common:1; Rare:23 | ||||
| chr17:7242234-7242257 | Rare:5 |