| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:56451320-56451562 | Common:1; Rare:64 | ||||
| chr16:57447359-57447491 | Common:2; Rare:35; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:70523538-70523834 | Common:3; Rare:92 | ||||
| chr16:75647647-75647824 | Common:2; Rare:79; Clinvar:2 | ||||
| chr16:85799509-85799702 | Common:2; Rare:56 | ||||
| chr17:28335451-28335781 | Common:1; Rare:75 | ||||
| chr17:28357509-28357658 | Rare:70 | ||||
| chr17:42609362-42609664 | Common:5; Rare:112 | ||||
| chr17:45061107-45061339 | Common:1; Rare:65 | ||||
| chr17:47831516-47831623 | Rare:28 | ||||
| chr17:59707402-59707665 | Common:3; Rare:74; Clinvar (benign):2 | ||||
| chr17:75046943-75047194 | Common:1; Rare:75 | ||||
| chr17:75261604-75261930 | Common:4; Rare:97; Clinvar (benign):2 | ||||
| chr17:75979126-75979272 | Rare:38; Clinvar:4 | ||||
| chr17:81703292-81703496 | Common:2; Rare:57; Clinvar (benign):2 |