| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:68291211-68291507 | Common:1; Rare:85 | ||||
| chr17:68511660-68512081 | Common:2; Rare:120 | ||||
| chr17:69327091-69327271 | Common:2; Rare:58 | ||||
| chr17:70169338-70169539 | Common:1; Rare:54 | ||||
| chr17:73232226-73232707 | Common:3; Rare:173 | ||||
| chr17:73311924-73312232 | Rare:80 | ||||
| chr17:74213319-74213578 | Common:4; Rare:56 | ||||
| chr17:74776287-74776540 | Common:4; Rare:83 | ||||
| chr17:75012565-75012689 | Common:1; Rare:31 | ||||
| chr17:75046929-75047194 | Common:1; Rare:81 | ||||
| chr17:75087787-75087978 | Common:2; Rare:47 | ||||
| chr17:75109843-75109994 | Common:2; Rare:46 | ||||
| chr17:75131675-75132058 | Common:5; Rare:140 | ||||
| chr17:75205370-75205749 | Common:1; Rare:122 | ||||
| chr17:75261583-75261967 | Common:4; Rare:129; Clinvar (benign):4 |