| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:19648657-19649010 | Common:3; Rare:126; Clinvar (benign):1 | ||||
| chr17:19977789-19977974 | Common:1; Rare:64 | ||||
| chr17:20009186-20009392 | Common:2; Rare:66 | ||||
| chr17:20155755-20156150 | Common:1; Rare:121 | ||||
| chr17:21019131-21019223 | Rare:28 | ||||
| chr17:21214140-21214365 | Common:2; Rare:100 | ||||
| chr17:27293991-27294226 | Common:2; Rare:89 | ||||
| chr17:27294304-27294435 | Common:1; Rare:35 | ||||
| chr17:27800500-27800790 | Common:1; Rare:47 | ||||
| chr17:28042156-28042276 | Rare:43 | ||||
| chr17:28335371-28335824 | Common:1; Rare:108 | ||||
| chr17:28357292-28357667 | Common:11; Rare:165 | ||||
| chr17:28571497-28571664 | Rare:39 | ||||
| chr17:28598994-28599165 | Common:2; Rare:47 | ||||
| chr17:28645091-28645318 | Common:1; Rare:85 |