| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:35537634-35537816 | Common:4; Rare:23 | ||||
| chr17:35578486-35578707 | Common:1; Rare:59; Clinvar:1; Clinvar (benign):1 | ||||
| chr17:35587184-35587547 | Rare:91 | ||||
| chr17:35986593-35986853 | Common:1; Rare:65 | ||||
| chr17:36103800-36103843 | Common:1; Rare:8 | ||||
| chr17:36196752-36196812 | Rare:4 | ||||
| chr17:36210800-36211068 | Rare:27 | ||||
| chr17:36486476-36486702 | Common:2; Rare:74 | ||||
| chr17:36534799-36535052 | Common:3; Rare:107 | ||||
| chr17:36544761-36545006 | Common:5; Rare:83 | ||||
| chr17:36601491-36601617 | Rare:39 | ||||
| chr17:36949053-36949213 | Rare:63 | ||||
| chr17:37359072-37359451 | Common:1; Rare:116 | ||||
| chr17:37406792-37406944 | Rare:62 | ||||
| chr17:37489736-37489919 | Rare:68 |