| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:17236660-17236804 | Rare:27 | ||||
| chr17:17236986-17237417 | Common:4; Rare:123; Clinvar:1; Clinvar (benign):3 | ||||
| chr17:17237642-17237762 | Rare:38 | ||||
| chr17:17280639-17280985 | Common:5; Rare:140 | ||||
| chr17:17281157-17281455 | Common:1; Rare:108 | ||||
| chr17:17303053-17303470 | Common:6; Rare:127 | ||||
| chr17:17303528-17303700 | Rare:65 | ||||
| chr17:17303731-17303884 | Rare:62 | ||||
| chr17:17476846-17477093 | Common:3; Rare:75 | ||||
| chr17:17496310-17496580 | Common:4; Rare:86 | ||||
| chr17:17591231-17592027 | Common:4; Rare:238 | ||||
| chr17:17592060-17592170 | Common:2; Rare:39 | ||||
| chr17:17681352-17681521 | Common:1; Rare:81 | ||||
| chr17:17681535-17681655 | Rare:26 | ||||
| chr17:17681741-17682132 | Common:3; Rare:120 |