| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:34156739-34156888 | Rare:20 | ||||
| chr17:34255133-34255293 | Rare:42 | ||||
| chr17:34961422-34961589 | Common:1; Rare:85 | ||||
| chr17:34980443-34980613 | Common:4; Rare:49 | ||||
| chr17:35242901-35243087 | Rare:62 | ||||
| chr17:35578511-35578721 | Common:1; Rare:58; Clinvar:1; Clinvar (benign):1 | ||||
| chr17:35587184-35587623 | Rare:107 | ||||
| chr17:35809305-35809575 | Rare:112 | ||||
| chr17:36534787-36535033 | Common:3; Rare:106 | ||||
| chr17:36544796-36544961 | Common:2; Rare:52 | ||||
| chr17:36601518-36601616 | Rare:26 | ||||
| chr17:36948768-36949038 | Common:2; Rare:92 | ||||
| chr17:37406812-37406924 | Rare:42 | ||||
| chr17:37609351-37609578 | Common:1; Rare:94 | ||||
| chr17:37643416-37643488 | Rare:33 |