| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:35373580-35373868 | Common:5; Rare:59 | ||||
| chr17:35578531-35578715 | Common:1; Rare:48; Clinvar (benign):1 | ||||
| chr17:35587188-35587502 | Rare:84 | ||||
| chr17:35809397-35809591 | Rare:98 | ||||
| chr17:36090131-36090338 | Common:1; Rare:39 | ||||
| chr17:36534805-36535034 | Common:3; Rare:103 | ||||
| chr17:36544787-36544968 | Common:3; Rare:60 | ||||
| chr17:36545406-36545654 | Common:2; Rare:80 | ||||
| chr17:37359108-37359430 | Rare:94 | ||||
| chr17:37406735-37406924 | Rare:77 | ||||
| chr17:37489704-37489911 | Rare:82 | ||||
| chr17:37609361-37609561 | Common:1; Rare:87 | ||||
| chr17:38428309-38428488 | Common:8; Rare:69 | ||||
| chr17:38706095-38706220 | Rare:45 | ||||
| chr17:38825270-38825427 | Common:2; Rare:48 |