| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:2645921-2646148 | Rare:39 | ||||
| chr17:2650668-2650821 | Common:1; Rare:32 | ||||
| chr17:2944017-2944152 | Common:3; Rare:23 | ||||
| chr17:2955289-2955468 | Rare:23 | ||||
| chr17:3650809-3650845 | Rare:10 | ||||
| chr17:3652604-3652726 | Common:1; Rare:21 | ||||
| chr17:3654707-3655055 | Common:1; Rare:94 | ||||
| chr17:3655081-3655381 | Common:3; Rare:111; Clinvar:6; Clinvar (benign):3; Clinvar (pathogenic):4 | ||||
| chr17:3656189-3656550 | Common:9; Rare:42; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
| chr17:3656953-3657030 | Rare:18 | ||||
| chr17:3659584-3659948 | Common:2; Rare:123; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):5 | ||||
| chr17:3663855-3663964 | Rare:28 | ||||
| chr17:3665013-3665385 | Common:13; Rare:71 | ||||
| chr17:3843119-3843229 | Common:1; Rare:29 | ||||
| chr17:4061829-4061890 | Rare:9 |