| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:7394962-7395093 | Rare:20 | ||||
| chr17:7404041-7404374 | Common:1; Rare:102 | ||||
| chr17:7404497-7404735 | Common:2; Rare:64 | ||||
| chr17:7404759-7404961 | Common:4; Rare:52 | ||||
| chr17:7435405-7435516 | Common:1; Rare:23 | ||||
| chr17:7438125-7438311 | Common:1; Rare:39 | ||||
| chr17:7440063-7440222 | Rare:27 | ||||
| chr17:7440330-7440888 | Rare:109 | ||||
| chr17:7441107-7441341 | Common:1; Rare:33 | ||||
| chr17:7444916-7445105 | Rare:45 | ||||
| chr17:7455380-7455680 | Common:4; Rare:83; Clinvar:2; Clinvar (benign):2 | ||||
| chr17:7455749-7455808 | Rare:18; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr17:7479427-7479826 | Common:6; Rare:69 | ||||
| chr17:7479927-7479973 | Rare:12 | ||||
| chr17:7483757-7484043 | Common:6; Rare:70 |