| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:714769-714947 | Common:3; Rare:58 | ||||
| chr17:732319-732615 | Common:2; Rare:103 | ||||
| chr17:752222-752315 | Common:2; Rare:37 | ||||
| chr17:997046-997218 | Common:1; Rare:89 | ||||
| chr17:1051001-1051218 | Common:1; Rare:40 | ||||
| chr17:1108937-1109439 | Common:2; Rare:151 | ||||
| chr17:1115287-1115616 | Common:2; Rare:63 | ||||
| chr17:1467846-1468052 | Rare:90; Clinvar (benign):3 | ||||
| chr17:1480576-1480849 | Common:2; Rare:85; Clinvar (benign):1 | ||||
| chr17:1492674-1492759 | Rare:16 | ||||
| chr17:1516588-1516971 | Common:2; Rare:134 | ||||
| chr17:1661638-1661992 | Common:2; Rare:82; Clinvar:2; Clinvar (benign):2 | ||||
| chr17:1710229-1710463 | Rare:66 | ||||
| chr17:1716145-1716544 | Common:3; Rare:126 | ||||
| chr17:1776929-1777243 | Common:1; Rare:102; Clinvar:1 |