| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:42017382-42017487 | Rare:47 | ||||
| chr17:42423047-42423462 | Common:1; Rare:115; Clinvar:2 | ||||
| chr17:42458748-42458945 | Common:3; Rare:74 | ||||
| chr17:42577680-42577849 | Rare:82 | ||||
| chr17:42609316-42609732 | Common:8; Rare:174; Clinvar (benign):2 | ||||
| chr17:42761027-42761254 | Rare:65 | ||||
| chr17:42798661-42798781 | Rare:39 | ||||
| chr17:42833378-42833487 | Rare:44 | ||||
| chr17:42964428-42964534 | Rare:50 | ||||
| chr17:42980444-42980571 | Common:1; Rare:43 | ||||
| chr17:42998702-42998787 | Rare:21 | ||||
| chr17:43125466-43125678 | Rare:49; Clinvar (benign):1 | ||||
| chr17:43170277-43170720 | Common:3; Rare:86 | ||||
| chr17:43171008-43171245 | Rare:76 | ||||
| chr17:43778907-43779041 | Rare:29 |