| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:42566947-42567116 | Common:3; Rare:57 | ||||
| chr17:42577682-42577844 | Rare:77 | ||||
| chr17:42609320-42609740 | Common:8; Rare:178; Clinvar (benign):2 | ||||
| chr17:42659508-42659541 | Rare:6 | ||||
| chr17:42676009-42676088 | Rare:15 | ||||
| chr17:42676955-42677279 | Common:1; Rare:88 | ||||
| chr17:42745013-42745114 | Common:2; Rare:38 | ||||
| chr17:42761027-42761276 | Rare:72 | ||||
| chr17:42798643-42798881 | Rare:71 | ||||
| chr17:42833351-42833485 | Rare:51 | ||||
| chr17:42964428-42964534 | Rare:50 | ||||
| chr17:43125330-43125654 | Rare:82; Clinvar:3; Clinvar (benign):3 | ||||
| chr17:43170284-43170712 | Common:3; Rare:83 | ||||
| chr17:43170982-43171245 | Rare:85 | ||||
| chr17:43398878-43398994 | Common:1; Rare:33 |