| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:43170284-43170511 | Common:2; Rare:46 | ||||
| chr17:43171037-43171245 | Rare:63 | ||||
| chr17:43211750-43211890 | Common:1; Rare:31 | ||||
| chr17:44070612-44070947 | Common:3; Rare:116; Clinvar:4; Clinvar (benign):2 | ||||
| chr17:44141901-44141972 | Rare:23 | ||||
| chr17:44186682-44187022 | Common:1; Rare:114 | ||||
| chr17:44324765-44325003 | Common:2; Rare:86 | ||||
| chr17:44345072-44345321 | Rare:52; Clinvar:5; Clinvar (benign):3 | ||||
| chr17:44503377-44503713 | Rare:132 | ||||
| chr17:44899374-44899729 | Common:2; Rare:111; Clinvar:1; Clinvar (benign):1 | ||||
| chr17:45060971-45061339 | Common:2; Rare:97 | ||||
| chr17:45148159-45148479 | Common:1; Rare:93 | ||||
| chr17:45490693-45490887 | Common:1; Rare:65 | ||||
| chr17:46193509-46193601 | Common:1; Rare:31 | ||||
| chr17:46225359-46225488 | Common:2; Rare:35 |