| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:35373476-35373993 | Common:6; Rare:106 | ||||
| chr17:35432468-35432797 | Common:1; Rare:54 | ||||
| chr17:35433103-35433391 | Common:6; Rare:61 | ||||
| chr17:35448230-35448653 | Common:2; Rare:99 | ||||
| chr17:35448678-35448998 | Common:4; Rare:64 | ||||
| chr17:35487218-35487433 | Rare:44 | ||||
| chr17:35487812-35487884 | Rare:26 | ||||
| chr17:35537642-35537935 | Common:4; Rare:41 | ||||
| chr17:35577935-35578034 | Common:1; Rare:32; Clinvar:4; Clinvar (pathogenic):2 | ||||
| chr17:35578429-35578832 | Common:3; Rare:93; Clinvar:3; Clinvar (benign):2 | ||||
| chr17:35587164-35587557 | Rare:99 | ||||
| chr17:35587716-35587806 | Rare:18 | ||||
| chr17:35808951-35809109 | Common:2; Rare:25 | ||||
| chr17:35809265-35809556 | Rare:124 | ||||
| chr17:35809683-35809750 | Rare:20 |