| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:44219425-44219698 | Rare:100 | ||||
| chr17:44219712-44220226 | Common:5; Rare:171 | ||||
| chr17:44220357-44220670 | Common:3; Rare:105 | ||||
| chr17:44220792-44220899 | Rare:32 | ||||
| chr17:44220957-44221079 | Rare:48 | ||||
| chr17:44221275-44221469 | Rare:56 | ||||
| chr17:44222067-44222248 | Rare:39 | ||||
| chr17:44324770-44325003 | Common:2; Rare:84 | ||||
| chr17:44345053-44345357 | Rare:69; Clinvar:5; Clinvar (benign):4 | ||||
| chr17:44385335-44385692 | Common:5; Rare:114; Clinvar:4 | ||||
| chr17:44503231-44503518 | Rare:101 | ||||
| chr17:44503533-44503752 | Rare:81 | ||||
| chr17:44503827-44503872 | Rare:8 | ||||
| chr17:44557010-44557275 | Rare:47 | ||||
| chr17:44557321-44557591 | Common:1; Rare:66 |