| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:45112907-45113152 | Common:1; Rare:89 | ||||
| chr17:45132333-45132635 | Common:2; Rare:90 | ||||
| chr17:45148109-45148637 | Common:1; Rare:175 | ||||
| chr17:45161482-45161939 | Common:1; Rare:119 | ||||
| chr17:45490708-45490867 | Rare:55 | ||||
| chr17:45894247-45894610 | Common:3; Rare:109; Clinvar:4; Clinvar (benign):2 | ||||
| chr17:46192775-46193019 | Common:3; Rare:61; Clinvar (benign):2 | ||||
| chr17:46193330-46193605 | Common:5; Rare:79 | ||||
| chr17:46225353-46225476 | Common:1; Rare:32 | ||||
| chr17:46922869-46923187 | Common:3; Rare:89; Clinvar:1; Clinvar (benign):7 | ||||
| chr17:47189102-47189143 | Rare:11 | ||||
| chr17:47189159-47189582 | Common:1; Rare:111 | ||||
| chr17:47323899-47324019 | Common:1; Rare:39 | ||||
| chr17:47649511-47649980 | Common:1; Rare:169 | ||||
| chr17:47831479-47831636 | Rare:50 |