| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:73192817-73193065 | Common:15; Rare:98; Clinvar:2; Clinvar (benign):1 | ||||
| chr17:73232096-73232715 | Common:4; Rare:236 | ||||
| chr17:74203427-74203770 | Common:3; Rare:103 | ||||
| chr17:74213319-74213578 | Common:4; Rare:56 | ||||
| chr17:74466426-74466659 | Rare:53 | ||||
| chr17:74776281-74776540 | Common:4; Rare:87 | ||||
| chr17:74972700-74972858 | Common:2; Rare:41 | ||||
| chr17:75012565-75012712 | Common:2; Rare:43 | ||||
| chr17:75046929-75047180 | Common:1; Rare:75 | ||||
| chr17:75109853-75109981 | Common:2; Rare:35 | ||||
| chr17:75130801-75131084 | Common:2; Rare:102 | ||||
| chr17:75154341-75154528 | Rare:83 | ||||
| chr17:75205360-75205730 | Common:1; Rare:112 | ||||
| chr17:75261590-75261935 | Common:4; Rare:108; Clinvar (benign):2 | ||||
| chr17:75271154-75271398 | Common:3; Rare:45 |