| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:7145549-7146256 | Common:6; Rare:180 | ||||
| chr17:7214604-7214851 | Rare:48 | ||||
| chr17:7214943-7215290 | Common:4; Rare:79 | ||||
| chr17:7215800-7215966 | Rare:18 | ||||
| chr17:7330093-7330317 | Common:3; Rare:41 | ||||
| chr17:7330355-7330463 | Common:4; Rare:27 | ||||
| chr17:7436446-7437333 | Common:5; Rare:425 | ||||
| chr17:7483327-7483518 | Common:1; Rare:34 | ||||
| chr17:7561049-7561206 | Common:1; Rare:29 | ||||
| chr17:7656851-7657351 | Common:4; Rare:236 | ||||
| chr17:7689101-7689501 | Common:4; Rare:102; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr17:7703589-7703849 | Common:1; Rare:43 | ||||
| chr17:7834932-7835337 | Common:2; Rare:231 | ||||
| chr17:7835506-7835885 | Common:7; Rare:116 | ||||
| chr17:7836331-7836455 | Common:1; Rare:39 |