| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:1829768-1830100 | Common:8; Rare:140 | ||||
| chr17:2039812-2039930 | Common:1; Rare:43; Clinvar:1 | ||||
| chr17:2303465-2303626 | Rare:61 | ||||
| chr17:2303716-2303987 | Common:2; Rare:103 | ||||
| chr17:2330361-2330582 | Common:2; Rare:53 | ||||
| chr17:2336412-2336552 | Rare:59 | ||||
| chr17:2392656-2392998 | Common:7; Rare:158 | ||||
| chr17:2396780-2397060 | Common:2; Rare:67 | ||||
| chr17:2511779-2512021 | Common:2; Rare:72 | ||||
| chr17:2593507-2593658 | Common:2; Rare:48 | ||||
| chr17:2593856-2593990 | Common:1; Rare:38; Clinvar:3; Clinvar (benign):3 | ||||
| chr17:2711742-2712033 | Common:2; Rare:83 | ||||
| chr17:2796357-2796478 | Rare:36 | ||||
| chr17:3636241-3636572 | Common:6; Rare:89; Clinvar:1; Clinvar (benign):2 | ||||
| chr17:3668527-3668861 | Common:3; Rare:140 |