| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:29140368-29140470 | Common:3; Rare:35 | ||||
| chr17:29568514-29568746 | Common:2; Rare:77 | ||||
| chr17:30291908-30292216 | Common:2; Rare:105 | ||||
| chr17:30824635-30824865 | Common:3; Rare:95 | ||||
| chr17:30906205-30906394 | Common:1; Rare:49 | ||||
| chr17:31273627-31273870 | Common:1; Rare:39 | ||||
| chr17:31314066-31314171 | Rare:22 | ||||
| chr17:31321588-31321761 | Common:3; Rare:26 | ||||
| chr17:32350012-32350228 | Rare:110 | ||||
| chr17:34961489-34961575 | Common:1; Rare:43 | ||||
| chr17:34980390-34980618 | Common:4; Rare:67 | ||||
| chr17:35242910-35243087 | Rare:60 | ||||
| chr17:35373615-35373841 | Common:4; Rare:44 | ||||
| chr17:35578511-35578699 | Common:1; Rare:52; Clinvar:1; Clinvar (benign):1 | ||||
| chr17:35880355-35880585 | Common:2; Rare:42 |