| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:42659291-42659434 | Rare:47 | ||||
| chr17:42682350-42682632 | Common:1; Rare:60 | ||||
| chr17:42773370-42773527 | Rare:45 | ||||
| chr17:42780347-42780658 | Common:2; Rare:94 | ||||
| chr17:42798651-42798793 | Rare:49 | ||||
| chr17:42833365-42833693 | Common:2; Rare:103 | ||||
| chr17:42834511-42834874 | Rare:78 | ||||
| chr17:42964109-42964544 | Common:5; Rare:179 | ||||
| chr17:42980384-42980586 | Common:1; Rare:64 | ||||
| chr17:42980798-42981055 | Common:1; Rare:62 | ||||
| chr17:42998049-42998557 | Common:5; Rare:121 | ||||
| chr17:43125317-43125718 | Rare:102; Clinvar:3; Clinvar (benign):3 | ||||
| chr17:43170192-43170517 | Common:2; Rare:71 | ||||
| chr17:43171004-43171299 | Common:1; Rare:101 | ||||
| chr17:43211674-43211909 | Common:2; Rare:55 |