| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:41966580-41966869 | Common:2; Rare:97 | ||||
| chr17:42017125-42017520 | Common:1; Rare:125 | ||||
| chr17:42017554-42017670 | Rare:36 | ||||
| chr17:42017676-42017735 | Rare:13 | ||||
| chr17:42121314-42121423 | Common:1; Rare:31 | ||||
| chr17:42154908-42155270 | Common:4; Rare:98 | ||||
| chr17:42287319-42287447 | Common:1; Rare:38 | ||||
| chr17:42423093-42423427 | Common:1; Rare:86; Clinvar:2 | ||||
| chr17:42458738-42458961 | Common:3; Rare:84 | ||||
| chr17:42566974-42567159 | Common:3; Rare:63 | ||||
| chr17:42577663-42577864 | Common:1; Rare:98 | ||||
| chr17:42609237-42609777 | Common:9; Rare:221; Clinvar (benign):2 | ||||
| chr17:42659162-42659470 | Rare:95 | ||||
| chr17:42676615-42676693 | Rare:12 | ||||
| chr17:42682388-42682548 | Rare:33 |