| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:75046929-75047191 | Common:1; Rare:79 | ||||
| chr17:75109893-75109988 | Common:1; Rare:26 | ||||
| chr17:75130753-75131101 | Common:2; Rare:124 | ||||
| chr17:75131441-75131860 | Common:5; Rare:168 | ||||
| chr17:75154405-75154836 | Common:1; Rare:140 | ||||
| chr17:75205370-75205750 | Common:1; Rare:122 | ||||
| chr17:75261570-75261971 | Common:4; Rare:138; Clinvar (benign):4 | ||||
| chr17:75271139-75271384 | Common:3; Rare:45 | ||||
| chr17:75289387-75289628 | Common:1; Rare:75; Clinvar:1; Clinvar (benign):1 | ||||
| chr17:75393565-75394077 | Common:1; Rare:132 | ||||
| chr17:75515427-75515657 | Common:3; Rare:67 | ||||
| chr17:75516402-75516563 | Rare:47; Clinvar (pathogenic):1 | ||||
| chr17:75525483-75525775 | Common:2; Rare:95 | ||||
| chr17:75639887-75640208 | Common:3; Rare:82 | ||||
| chr17:75667131-75667423 | Common:4; Rare:100 |