| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:41688613-41689026 | Common:3; Rare:170 | ||||
| chr17:41812577-41813019 | Common:3; Rare:96; Clinvar:5 | ||||
| chr17:41966614-41966837 | Common:1; Rare:80 | ||||
| chr17:42017387-42017482 | Rare:42 | ||||
| chr17:42111945-42112082 | Rare:27 | ||||
| chr17:42535974-42536279 | Common:3; Rare:91; Clinvar:8; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr17:42567004-42567149 | Common:3; Rare:45 | ||||
| chr17:42577651-42577838 | Rare:89 | ||||
| chr17:42609258-42609744 | Common:9; Rare:206; Clinvar (benign):2 | ||||
| chr17:42682355-42682602 | Rare:51 | ||||
| chr17:42798618-42798792 | Rare:62 | ||||
| chr17:42833348-42833498 | Rare:56 | ||||
| chr17:42964433-42964557 | Common:1; Rare:54 | ||||
| chr17:42980394-42980576 | Common:1; Rare:57 | ||||
| chr17:43125338-43125694 | Rare:88; Clinvar:3; Clinvar (benign):2 |