| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:43170284-43170712 | Common:3; Rare:83 | ||||
| chr17:43171016-43171267 | Common:1; Rare:84 | ||||
| chr17:43778850-43779078 | Rare:55 | ||||
| chr17:43833109-43833273 | Rare:48 | ||||
| chr17:43847016-43847184 | Rare:37 | ||||
| chr17:44070636-44070993 | Common:3; Rare:126; Clinvar:4; Clinvar (benign):2 | ||||
| chr17:44123585-44123824 | Common:3; Rare:70 | ||||
| chr17:44186668-44187002 | Common:1; Rare:119 | ||||
| chr17:44187149-44187274 | Rare:33 | ||||
| chr17:44221279-44221427 | Rare:43 | ||||
| chr17:44324748-44324993 | Common:3; Rare:92 | ||||
| chr17:44503369-44503713 | Rare:134 | ||||
| chr17:44899367-44899741 | Common:2; Rare:117; Clinvar:2; Clinvar (benign):1 | ||||
| chr17:45060992-45061361 | Common:2; Rare:106 | ||||
| chr17:45132331-45132631 | Common:2; Rare:89 |