| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:44221232-44221439 | Rare:58 | ||||
| chr17:44222068-44222269 | Rare:43 | ||||
| chr17:44308441-44308619 | Common:1; Rare:54 | ||||
| chr17:44324728-44324976 | Common:3; Rare:94 | ||||
| chr17:44345022-44345327 | Rare:67; Clinvar:5; Clinvar (benign):3 | ||||
| chr17:44385335-44385582 | Common:4; Rare:73; Clinvar:1 | ||||
| chr17:44503345-44503766 | Rare:158 | ||||
| chr17:44708764-44708924 | Common:3; Rare:56 | ||||
| chr17:44775650-44775938 | Common:3; Rare:51 | ||||
| chr17:44829583-44829828 | Common:1; Rare:64 | ||||
| chr17:44899359-44899736 | Common:2; Rare:114; Clinvar:1; Clinvar (benign):1 | ||||
| chr17:44911505-44911583 | Common:2; Rare:20; Clinvar:1 | ||||
| chr17:44947586-44947954 | Common:1; Rare:93 | ||||
| chr17:45051415-45051688 | Common:1; Rare:90 | ||||
| chr17:45060922-45061339 | Common:3; Rare:105 |