| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:13601864-13602177 | Common:3; Rare:100 | ||||
| chr17:14069341-14069580 | Common:2; Rare:84; Clinvar:3; Clinvar (benign):3 | ||||
| chr17:14300731-14301036 | Rare:71 | ||||
| chr17:14301561-14301818 | Common:2; Rare:110 | ||||
| chr17:15260740-15260935 | Common:1; Rare:72; Clinvar (benign):3 | ||||
| chr17:15262493-15262689 | Rare:49 | ||||
| chr17:15563432-15563754 | Common:1; Rare:106 | ||||
| chr17:15684279-15684388 | Common:1; Rare:36 | ||||
| chr17:15699532-15699773 | Common:3; Rare:66 | ||||
| chr17:15999593-16000086 | Common:4; Rare:203; Clinvar:6; Clinvar (benign):13; Clinvar (pathogenic):2 | ||||
| chr17:16024916-16025142 | Common:1; Rare:64; Clinvar:2; Clinvar (benign):2 | ||||
| chr17:16039534-16039951 | Common:2; Rare:93 | ||||
| chr17:16040440-16040571 | Rare:24 | ||||
| chr17:16058231-16058525 | Common:1; Rare:53 | ||||
| chr17:16215532-16215657 | Common:1; Rare:52 |