| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:42744998-42745157 | Common:3; Rare:62 | ||||
| chr17:42761178-42761328 | Common:1; Rare:58 | ||||
| chr17:42773346-42773488 | Rare:41 | ||||
| chr17:42773548-42773960 | Common:2; Rare:174 | ||||
| chr17:42798654-42798762 | Rare:36 | ||||
| chr17:42824233-42824440 | Common:1; Rare:59 | ||||
| chr17:42833062-42833469 | Rare:114 | ||||
| chr17:42964442-42964564 | Common:1; Rare:50 | ||||
| chr17:42980394-42980622 | Common:1; Rare:89 | ||||
| chr17:42997989-42998273 | Common:2; Rare:44 | ||||
| chr17:42998332-42998478 | Common:3; Rare:48 | ||||
| chr17:43022330-43022570 | Rare:69 | ||||
| chr17:43024490-43024860 | Common:3; Rare:56 | ||||
| chr17:43025084-43025252 | Rare:37 | ||||
| chr17:43125244-43125610 | Rare:93; Clinvar:7; Clinvar (benign):10 |