| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:28894012-28894157 | Common:1; Rare:25 | ||||
| chr17:29723013-29723038 | Rare:4 | ||||
| chr17:29727003-29727068 | Rare:18 | ||||
| chr17:30600649-30600901 | Common:2; Rare:76 | ||||
| chr17:30602325-30602426 | Rare:22 | ||||
| chr17:30804032-30804242 | Rare:41 | ||||
| chr17:30953088-30953337 | Common:1; Rare:53 | ||||
| chr17:31008519-31008605 | Common:1; Rare:19 | ||||
| chr17:31008613-31008721 | Common:1; Rare:28 | ||||
| chr17:31305323-31305916 | Common:2; Rare:121; Clinvar (benign):1 | ||||
| chr17:32127451-32127640 | Rare:50 | ||||
| chr17:32523444-32523561 | Rare:24 | ||||
| chr17:35089899-35089935 | Rare:5 | ||||
| chr17:35242307-35242433 | Rare:19 | ||||
| chr17:35313183-35313537 | Rare:71 |