| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:28727911-28728090 | Rare:40 | ||||
| chr17:28728092-28728200 | Rare:29 | ||||
| chr17:28728209-28728277 | Rare:13 | ||||
| chr17:28728488-28728824 | Rare:93; Clinvar (benign):1 | ||||
| chr17:28728860-28729130 | Common:2; Rare:70 | ||||
| chr17:28743431-28743654 | Rare:31 | ||||
| chr17:28743771-28744169 | Common:4; Rare:111 | ||||
| chr17:28744208-28744577 | Common:3; Rare:106 | ||||
| chr17:28744580-28744666 | Rare:13 | ||||
| chr17:28746773-28746948 | Common:1; Rare:36 | ||||
| chr17:28747038-28747262 | Rare:53 | ||||
| chr17:28811795-28811841 | Common:1; Rare:9 | ||||
| chr17:28812383-28812724 | Common:1; Rare:89 | ||||
| chr17:28812808-28812949 | Common:2; Rare:22 | ||||
| chr17:28842710-28842925 | Common:2; Rare:75 |