| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:72120792-72121047 | Rare:67 | ||||
| chr17:73232214-73232711 | Common:3; Rare:183 | ||||
| chr17:74776295-74776540 | Common:4; Rare:79 | ||||
| chr17:75012565-75012696 | Common:1; Rare:33 | ||||
| chr17:75130754-75131120 | Common:2; Rare:136 | ||||
| chr17:75261590-75261925 | Common:4; Rare:102; Clinvar (benign):1 | ||||
| chr17:75667173-75667403 | Common:4; Rare:79 | ||||
| chr17:75979074-75979276 | Rare:56; Clinvar:4 | ||||
| chr17:76103696-76103867 | Common:5; Rare:60 | ||||
| chr17:76384468-76384659 | Common:2; Rare:57 | ||||
| chr17:76725930-76726085 | Common:1; Rare:39 | ||||
| chr17:76726491-76726886 | Common:5; Rare:146 | ||||
| chr17:76737325-76737474 | Common:2; Rare:59 | ||||
| chr17:77320077-77320323 | Common:1; Rare:64; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr17:78187029-78187364 | Common:3; Rare:108 |