| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:4007870-4007957 | Rare:18 | ||||
| chr17:4123912-4124217 | Common:2; Rare:74 | ||||
| chr17:4126908-4127061 | Rare:27 | ||||
| chr17:4169275-4169492 | Common:3; Rare:61 | ||||
| chr17:4540704-4540851 | Common:1; Rare:39 | ||||
| chr17:4711300-4711664 | Common:1; Rare:64 | ||||
| chr17:4881032-4881178 | Rare:37 | ||||
| chr17:6476887-6477206 | Rare:99; Clinvar:4; Clinvar (benign):1 | ||||
| chr17:6657237-6657363 | Common:3; Rare:15 | ||||
| chr17:7174455-7174566 | Common:2; Rare:45 | ||||
| chr17:7310783-7311122 | Rare:86 | ||||
| chr17:7834106-7834251 | Rare:50 | ||||
| chr17:7835520-7835824 | Common:5; Rare:95 | ||||
| chr17:7836385-7836466 | Rare:14 | ||||
| chr17:7841136-7841271 | Rare:25 |