| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:44899362-44899798 | Common:3; Rare:132; Clinvar:3; Clinvar (benign):1 | ||||
| chr17:44911517-44911631 | Common:3; Rare:34; Clinvar:2 | ||||
| chr17:44968267-44968559 | Rare:77 | ||||
| chr17:45051416-45051686 | Common:1; Rare:90 | ||||
| chr17:45060928-45061457 | Common:3; Rare:152 | ||||
| chr17:45132509-45132631 | Common:1; Rare:41 | ||||
| chr17:45148142-45148604 | Common:1; Rare:155 | ||||
| chr17:45148714-45148840 | Rare:35 | ||||
| chr17:45161021-45161099 | Rare:14 | ||||
| chr17:45161494-45162011 | Common:1; Rare:127 | ||||
| chr17:45262137-45262212 | Rare:12 | ||||
| chr17:45317003-45317346 | Common:4; Rare:84 | ||||
| chr17:45425803-45425938 | Common:3; Rare:16 | ||||
| chr17:46192726-46193020 | Common:3; Rare:74; Clinvar (benign):4 | ||||
| chr17:46818720-46818809 | Rare:14 |