| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:75261469-75261986 | Common:4; Rare:183; Clinvar (benign):4 | ||||
| chr17:75270295-75270875 | Common:1; Rare:125 | ||||
| chr17:75271090-75271473 | Common:6; Rare:78 | ||||
| chr17:75288895-75289020 | Rare:20 | ||||
| chr17:75289153-75289266 | Common:1; Rare:26 | ||||
| chr17:75289296-75289883 | Common:6; Rare:158; Clinvar:1; Clinvar (benign):2 | ||||
| chr17:75393850-75394122 | Common:1; Rare:61 | ||||
| chr17:75404924-75405159 | Common:1; Rare:56 | ||||
| chr17:75405579-75405939 | Common:2; Rare:111 | ||||
| chr17:75456323-75456767 | Common:3; Rare:136 | ||||
| chr17:75515610-75515949 | Common:1; Rare:71 | ||||
| chr17:75516353-75516613 | Common:2; Rare:74; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr17:75516865-75517237 | Common:5; Rare:156; Clinvar:4; Clinvar (benign):9; Clinvar (pathogenic):1 | ||||
| chr17:75525444-75525753 | Common:3; Rare:99 | ||||
| chr17:75646137-75646404 | Common:5; Rare:60 |