| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:42798661-42798785 | Rare:40 | ||||
| chr17:42833359-42833461 | Rare:38 | ||||
| chr17:42964436-42964512 | Rare:36 | ||||
| chr17:43125359-43125586 | Rare:38; Clinvar:3; Clinvar (benign):2 | ||||
| chr17:43170972-43171245 | Rare:88 | ||||
| chr17:44111226-44111453 | Rare:62 | ||||
| chr17:44170507-44170715 | Rare:36 | ||||
| chr17:44186687-44187002 | Common:1; Rare:107 | ||||
| chr17:44187148-44187274 | Rare:33 | ||||
| chr17:44221236-44221319 | Rare:26 | ||||
| chr17:44324748-44324987 | Common:3; Rare:88 | ||||
| chr17:44503364-44503713 | Rare:135 | ||||
| chr17:44899383-44899720 | Common:2; Rare:103; Clinvar (benign):1 | ||||
| chr17:45060987-45061339 | Common:2; Rare:93 | ||||
| chr17:45148159-45148475 | Common:1; Rare:90 |