| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:30235695-30235844 | Rare:21; Clinvar:2 | ||||
| chr17:30824608-30824835 | Common:3; Rare:95 | ||||
| chr17:30906205-30906354 | Common:1; Rare:42 | ||||
| chr17:31321590-31321876 | Common:3; Rare:47 | ||||
| chr17:32342133-32342268 | Rare:34 | ||||
| chr17:32350011-32350228 | Rare:110 | ||||
| chr17:32444222-32444512 | Common:1; Rare:95 | ||||
| chr17:34255127-34255313 | Rare:48 | ||||
| chr17:34961489-34961564 | Common:1; Rare:36 | ||||
| chr17:34980382-34980607 | Common:4; Rare:65 | ||||
| chr17:34981146-34981188 | Rare:6 | ||||
| chr17:35242910-35243081 | Rare:57 | ||||
| chr17:35578486-35578728 | Common:2; Rare:63; Clinvar:1; Clinvar (benign):1 | ||||
| chr17:35587233-35587563 | Rare:79 | ||||
| chr17:36486475-36486724 | Common:3; Rare:89 |