| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:50373157-50373229 | Common:2; Rare:35 | ||||
| chr17:50707864-50708105 | Rare:51 | ||||
| chr17:50866346-50866641 | Common:3; Rare:87 | ||||
| chr17:51260341-51260581 | Common:3; Rare:104 | ||||
| chr17:54968608-54968772 | Common:3; Rare:81 | ||||
| chr17:56914016-56914176 | Rare:41 | ||||
| chr17:58692361-58692663 | Common:2; Rare:125; Clinvar:9; Clinvar (benign):19 | ||||
| chr17:59155146-59155448 | Common:2; Rare:73 | ||||
| chr17:59707378-59707744 | Common:4; Rare:102; Clinvar (benign):6 | ||||
| chr17:59892902-59893136 | Rare:66 | ||||
| chr17:60525936-60526311 | Common:2; Rare:128 | ||||
| chr17:61399521-61399920 | Common:1; Rare:110 | ||||
| chr17:62423809-62423916 | Rare:41 | ||||
| chr17:62627334-62627756 | Common:2; Rare:116 | ||||
| chr17:63773532-63773825 | Common:2; Rare:98 |