| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:34255093-34255333 | Rare:65 | ||||
| chr17:34961402-34961561 | Rare:74 | ||||
| chr17:35242910-35243086 | Rare:60 | ||||
| chr17:35578551-35578698 | Common:1; Rare:39; Clinvar (benign):1 | ||||
| chr17:35586992-35587497 | Common:2; Rare:126 | ||||
| chr17:36544833-36544961 | Common:1; Rare:40 | ||||
| chr17:37406770-37406935 | Rare:66 | ||||
| chr17:37489724-37489900 | Rare:69 | ||||
| chr17:38428318-38428472 | Common:8; Rare:63 | ||||
| chr17:38706096-38706248 | Rare:53 | ||||
| chr17:38825278-38825378 | Common:1; Rare:28 | ||||
| chr17:38853696-38853895 | Common:3; Rare:79 | ||||
| chr17:38869907-38870181 | Common:2; Rare:83 | ||||
| chr17:39451250-39451392 | Common:2; Rare:47 | ||||
| chr17:39637052-39637194 | Common:3; Rare:47 |