| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:14069225-14069746 | Common:3; Rare:163; Clinvar:4; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr17:14069867-14069930 | Rare:14 | ||||
| chr17:14300717-14301465 | Common:6; Rare:184 | ||||
| chr17:15260554-15260675 | Common:1; Rare:27; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr17:15260781-15260858 | Rare:29 | ||||
| chr17:15563034-15563114 | Rare:16 | ||||
| chr17:15563405-15563782 | Common:1; Rare:128 | ||||
| chr17:15650922-15651357 | Common:4; Rare:119 | ||||
| chr17:15651589-15652004 | Common:1; Rare:79 | ||||
| chr17:15684219-15684355 | Common:3; Rare:44 | ||||
| chr17:15699441-15699826 | Common:5; Rare:109 | ||||
| chr17:15944991-15945501 | Common:4; Rare:150 | ||||
| chr17:15999401-15999907 | Common:4; Rare:247; Clinvar:7; Clinvar (benign):10; Clinvar (pathogenic):2 | ||||
| chr17:15999971-16000243 | Common:1; Rare:90; Clinvar:2; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr17:16215013-16215149 | Rare:39 |