| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:77127650-77128007 | Common:1; Rare:71 | ||||
| chr17:77140415-77140434 | Rare:2 | ||||
| chr17:77140630-77141063 | Common:3; Rare:151 | ||||
| chr17:77319170-77319602 | Common:4; Rare:98; Clinvar (benign):3 | ||||
| chr17:77319642-77319961 | Common:1; Rare:71; Clinvar (benign):1 | ||||
| chr17:77320074-77320324 | Common:1; Rare:66; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr17:77323800-77323938 | Common:1; Rare:22 | ||||
| chr17:77372965-77373108 | Rare:43 | ||||
| chr17:77374440-77374514 | Rare:19 | ||||
| chr17:77400490-77400575 | Rare:17 | ||||
| chr17:77404913-77405113 | Common:3; Rare:42; Clinvar (benign):1 | ||||
| chr17:77450346-77450723 | Common:1; Rare:79 | ||||
| chr17:77453704-77453825 | Rare:23 | ||||
| chr17:77453915-77454118 | Common:2; Rare:47 | ||||
| chr17:78113552-78113902 | Common:1; Rare:98 |