| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:20494214-20494497 | Common:2; Rare:65 | ||||
| chr17:35567891-35568139 | Common:2; Rare:73 | ||||
| chr17:38452359-38452522 | Common:1; Rare:24 | ||||
| chr17:40518634-40518712 | Rare:17 | ||||
| chr17:41502980-41503349 | Common:3; Rare:103; Clinvar:3; Clinvar (benign):6 | ||||
| chr17:41518880-41519117 | Rare:38 | ||||
| chr17:41610852-41611101 | Rare:95; Clinvar:1 | ||||
| chr17:41620914-41621145 | Rare:77; Clinvar (pathogenic):1 | ||||
| chr17:41651500-41651872 | Common:1; Rare:88 | ||||
| chr17:41758502-41758819 | Common:2; Rare:72; Clinvar:10; Clinvar (benign):4 | ||||
| chr17:41784219-41784496 | Common:2; Rare:63 | ||||
| chr17:43002750-43003043 | Common:1; Rare:94 | ||||
| chr17:43315658-43315919 | Common:6; Rare:111 | ||||
| chr17:45247771-45247972 | Common:1; Rare:34 | ||||
| chr17:45248343-45248394 | Common:1; Rare:9 |