| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:50055694-50056182 | Common:6; Rare:108 | ||||
| chr17:50063953-50064166 | Common:1; Rare:40 | ||||
| chr17:50095075-50095376 | Common:1; Rare:86 | ||||
| chr17:50115878-50116051 | Common:2; Rare:59 | ||||
| chr17:50186639-50187153 | Common:2; Rare:153; Clinvar:8; Clinvar (benign):11; Clinvar (pathogenic):1 | ||||
| chr17:50187189-50187551 | Common:2; Rare:65; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr17:50188876-50189065 | Rare:50; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr17:50189082-50189937 | Common:4; Rare:196; Clinvar:8; Clinvar (benign):8; Clinvar (pathogenic):3 | ||||
| chr17:50192465-50192692 | Common:1; Rare:52; Clinvar:3; Clinvar (benign):6 | ||||
| chr17:50194525-50194825 | Common:3; Rare:92; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):4 | ||||
| chr17:50195416-50195691 | Rare:65; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr17:50196740-50197113 | Common:3; Rare:82; Clinvar:1; Clinvar (benign):2 | ||||
| chr17:50198109-50198525 | Common:2; Rare:89; Clinvar:3; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr17:50200143-50200415 | Common:3; Rare:58; Clinvar:1 | ||||
| chr17:50201390-50201690 | Common:2; Rare:89; Clinvar:4; Clinvar (benign):4 |