| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:13602380-13602640 | Common:2; Rare:126 | ||||
| chr17:14068656-14069296 | Common:15; Rare:137 | ||||
| chr17:14069281-14069611 | Common:6; Rare:276; Clinvar:9; Clinvar (benign):8; Clinvar (pathogenic):1 | ||||
| chr17:14300729-14301207 | Common:9; Rare:330 | ||||
| chr17:15260290-15260690 | Common:4; Rare:69; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr17:15260708-15261060 | Common:4; Rare:176; Clinvar (benign):6 | ||||
| chr17:15262498-15262778 | Rare:160 | ||||
| chr17:15265279-15265664 | Rare:71; Clinvar:1 | ||||
| chr17:15563432-15563782 | Common:2; Rare:207 | ||||
| chr17:15651526-15652243 | Common:4; Rare:223 | ||||
| chr17:15699441-15699823 | Common:9; Rare:186 | ||||
| chr17:15944580-15945330 | Common:8; Rare:364 | ||||
| chr17:15998743-15999510 | Common:7; Rare:375; Clinvar:6; Clinvar (benign):2 | ||||
| chr17:15999505-16000022 | Common:9; Rare:580; Clinvar:17; Clinvar (benign):29; Clinvar (pathogenic):6 | ||||
| chr17:16215364-16215814 | Common:6; Rare:377 |