| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:73192769-73193126 | Common:15; Rare:142; Clinvar:4; Clinvar (benign):1 | ||||
| chr17:73232210-73232673 | Common:2; Rare:163 | ||||
| chr17:74776240-74776520 | Common:4; Rare:89 | ||||
| chr17:75046939-75047201 | Common:1; Rare:77 | ||||
| chr17:75261577-75261981 | Common:4; Rare:139; Clinvar (benign):4 | ||||
| chr17:75393725-75394023 | Common:1; Rare:73 | ||||
| chr17:75515491-75515657 | Common:2; Rare:44 | ||||
| chr17:75516412-75516570 | Common:1; Rare:47; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr17:75667131-75667394 | Common:4; Rare:91 | ||||
| chr17:75779436-75779532 | Common:1; Rare:47 | ||||
| chr17:75979109-75979490 | Common:1; Rare:99; Clinvar:4; Clinvar (benign):1 | ||||
| chr17:76537703-76537957 | Rare:61 | ||||
| chr17:76726437-76726910 | Common:5; Rare:182 | ||||
| chr17:76737328-76737715 | Common:3; Rare:133 | ||||
| chr17:76737845-76738122 | Common:4; Rare:80 |