| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:68247854-68248139 | Common:12; Rare:235 | ||||
| chr17:68291089-68291755 | Common:5; Rare:311 | ||||
| chr17:68291835-68292235 | Common:6; Rare:174 | ||||
| chr17:68399340-68399680 | Common:7; Rare:90 | ||||
| chr17:68456460-68456990 | Common:3; Rare:137 | ||||
| chr17:68457906-68458066 | Common:2; Rare:39 | ||||
| chr17:68511765-68512253 | Common:3; Rare:195 | ||||
| chr17:68512310-68513080 | Common:2; Rare:485; Clinvar:4; Clinvar (benign):6 | ||||
| chr17:68514882-68515169 | Common:3; Rare:115 | ||||
| chr17:68525242-68526120 | Common:6; Rare:272; Clinvar:4; Clinvar (benign):16; Clinvar (pathogenic):6 | ||||
| chr17:68600118-68600409 | Common:2; Rare:111; Clinvar:1; Clinvar (benign):1 | ||||
| chr17:68601244-68601476 | Common:4; Rare:87 | ||||
| chr17:69327050-69327334 | Common:4; Rare:160 | ||||
| chr17:69414602-69414743 | Rare:48 | ||||
| chr17:72120773-72121175 | Rare:181; Clinvar:1 |