| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:34997406-34997746 | Common:2; Rare:73 | ||||
| chr17:35063662-35063836 | Rare:26 | ||||
| chr17:35242910-35243086 | Rare:60 | ||||
| chr17:35373610-35374035 | Common:5; Rare:89 | ||||
| chr17:35448344-35448514 | Common:1; Rare:34 | ||||
| chr17:35578492-35578684 | Common:1; Rare:47; Clinvar:1; Clinvar (benign):1 | ||||
| chr17:35587204-35587497 | Rare:78 | ||||
| chr17:35795599-35795731 | Rare:30 | ||||
| chr17:36486476-36486702 | Common:2; Rare:74 | ||||
| chr17:36534852-36534998 | Common:2; Rare:66 | ||||
| chr17:36544809-36545002 | Common:4; Rare:65 | ||||
| chr17:36601293-36601616 | Common:3; Rare:82 | ||||
| chr17:37406762-37406924 | Rare:69 | ||||
| chr17:37489704-37489907 | Rare:81 | ||||
| chr17:37609351-37609640 | Common:1; Rare:121 |