| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:44898819-44899219 | Common:7; Rare:143 | ||||
| chr17:44899375-44899812 | Common:3; Rare:130; Clinvar:3; Clinvar (benign):1 | ||||
| chr17:44947656-44947963 | Common:1; Rare:86 | ||||
| chr17:44968282-44968587 | Rare:81 | ||||
| chr17:45060494-45060894 | Rare:101 | ||||
| chr17:45060985-45061350 | Common:2; Rare:102 | ||||
| chr17:45132477-45132693 | Common:3; Rare:71 | ||||
| chr17:45148233-45148504 | Rare:100 | ||||
| chr17:45161474-45161634 | Rare:48 | ||||
| chr17:45316603-45316812 | Common:1; Rare:55 | ||||
| chr17:45316955-45317347 | Common:5; Rare:97 | ||||
| chr17:45425720-45426110 | Common:3; Rare:51 | ||||
| chr17:45490709-45490940 | Common:6; Rare:76 | ||||
| chr17:46192825-46193094 | Common:1; Rare:64 | ||||
| chr17:46193324-46193640 | Common:6; Rare:92 |