| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:35578539-35578715 | Common:1; Rare:45; Clinvar (benign):1 | ||||
| chr17:35587151-35587570 | Common:1; Rare:108 | ||||
| chr17:36486476-36486708 | Common:2; Rare:79 | ||||
| chr17:36534805-36535016 | Common:3; Rare:90 | ||||
| chr17:36544809-36544961 | Common:2; Rare:50 | ||||
| chr17:37406778-37406935 | Rare:63 | ||||
| chr17:37489709-37489919 | Rare:80 | ||||
| chr17:37609345-37609561 | Common:1; Rare:91 | ||||
| chr17:37643403-37643472 | Common:1; Rare:35 | ||||
| chr17:38428268-38428481 | Common:8; Rare:79 | ||||
| chr17:38604705-38605002 | Common:1; Rare:52 | ||||
| chr17:38752496-38752826 | Common:4; Rare:89 | ||||
| chr17:38825272-38825382 | Common:1; Rare:32 | ||||
| chr17:38853691-38853897 | Common:3; Rare:84 | ||||
| chr17:38869836-38870143 | Common:4; Rare:98 |