| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:70169319-70169554 | Common:1; Rare:63 | ||||
| chr17:72120793-72121029 | Rare:62 | ||||
| chr17:73164848-73165024 | Common:2; Rare:53 | ||||
| chr17:73192809-73193076 | Common:15; Rare:111; Clinvar:2; Clinvar (benign):1 | ||||
| chr17:73232181-73232711 | Common:3; Rare:197 | ||||
| chr17:73311953-73312206 | Rare:66 | ||||
| chr17:74213349-74213574 | Common:4; Rare:51 | ||||
| chr17:74431287-74431390 | Rare:25 | ||||
| chr17:74466578-74466687 | Rare:33 | ||||
| chr17:74776288-74776550 | Common:4; Rare:84 | ||||
| chr17:75012565-75012719 | Common:2; Rare:46 | ||||
| chr17:75046929-75047116 | Common:1; Rare:57 | ||||
| chr17:75182836-75183153 | Common:2; Rare:114 | ||||
| chr17:75205370-75205749 | Common:1; Rare:122 | ||||
| chr17:75261590-75261935 | Common:4; Rare:108; Clinvar (benign):2 |