| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:2711576-2712043 | Common:4; Rare:226 | ||||
| chr17:2796179-2796472 | Common:2; Rare:121 | ||||
| chr17:3636218-3636546 | Common:9; Rare:188; Clinvar (benign):3 | ||||
| chr17:3636593-3636789 | Common:2; Rare:56; Clinvar:3; Clinvar (benign):2 | ||||
| chr17:3668508-3668872 | Common:6; Rare:283 | ||||
| chr17:3695140-3695590 | Common:4; Rare:157 | ||||
| chr17:3695604-3696004 | Common:3; Rare:135 | ||||
| chr17:3696013-3696303 | Common:1; Rare:78 | ||||
| chr17:3723756-3723929 | Common:2; Rare:192 | ||||
| chr17:3845830-3846120 | Common:1; Rare:77 | ||||
| chr17:3846221-3846449 | Common:1; Rare:67 | ||||
| chr17:3892907-3893268 | Common:6; Rare:224 | ||||
| chr17:3916458-3916626 | Common:1; Rare:37 | ||||
| chr17:3964310-3964690 | Common:4; Rare:189 | ||||
| chr17:4142944-4143235 | Common:6; Rare:198 |