| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:35242943-35243081 | Rare:42 | ||||
| chr17:35373610-35373807 | Common:3; Rare:40 | ||||
| chr17:35433143-35433465 | Common:5; Rare:73 | ||||
| chr17:35578539-35578694 | Common:1; Rare:39; Clinvar (benign):1 | ||||
| chr17:35587194-35587525 | Rare:86 | ||||
| chr17:35809305-35809518 | Rare:80 | ||||
| chr17:36486496-36486692 | Common:2; Rare:67 | ||||
| chr17:36534795-36535016 | Common:3; Rare:92 | ||||
| chr17:36544809-36544961 | Common:2; Rare:50 | ||||
| chr17:37406799-37406924 | Rare:50 | ||||
| chr17:37609356-37609561 | Common:1; Rare:88 | ||||
| chr17:38296962-38297197 | Common:4; Rare:73 | ||||
| chr17:38428258-38428485 | Common:8; Rare:82 | ||||
| chr17:38825268-38825389 | Common:2; Rare:38 | ||||
| chr17:38869836-38870143 | Common:4; Rare:98 |