| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:45149323-45149470 | Rare:52 | ||||
| chr17:45149887-45150106 | Rare:40 | ||||
| chr17:45151453-45151480 | Rare:3 | ||||
| chr17:45151715-45151778 | Rare:8 | ||||
| chr17:45226136-45226435 | Common:1; Rare:66 | ||||
| chr17:45228996-45229317 | Common:2; Rare:58 | ||||
| chr17:45242114-45242390 | Common:1; Rare:70 | ||||
| chr17:45247785-45247979 | Common:1; Rare:32 | ||||
| chr17:45248334-45248367 | Common:1; Rare:6 | ||||
| chr17:45585164-45585231 | Rare:5 | ||||
| chr17:45586200-45586487 | Common:4; Rare:35 | ||||
| chr17:46929373-46929580 | Common:1; Rare:65; Clinvar:7; Clinvar (benign):1 | ||||
| chr17:47100248-47100376 | Rare:37 | ||||
| chr17:47492466-47492508 | Common:1; Rare:20 | ||||
| chr17:47699180-47699321 | Rare:27 |