| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:181621-181765 | Rare:41 | ||||
| chr17:352310-352670 | Common:6; Rare:156 | ||||
| chr17:352727-353371 | Common:12; Rare:171 | ||||
| chr17:386101-386825 | Common:16; Rare:227 | ||||
| chr17:409923-410400 | Common:27; Rare:553 | ||||
| chr17:714689-715043 | Common:11; Rare:261; Clinvar (benign):2 | ||||
| chr17:732000-732770 | Common:7; Rare:461 | ||||
| chr17:752107-752496 | Common:8; Rare:380 | ||||
| chr17:782180-782620 | Common:8; Rare:527 | ||||
| chr17:979704-980044 | Common:9; Rare:388 | ||||
| chr17:996670-997014 | Common:3; Rare:120 | ||||
| chr17:997091-997197 | Common:1; Rare:60 | ||||
| chr17:1108310-1108810 | Rare:229 | ||||
| chr17:1108958-1109257 | Common:3; Rare:224 | ||||
| chr17:1109312-1109518 | Rare:102 |