| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:19377887-19378036 | Common:1; Rare:37 | ||||
| chr17:19378162-19378545 | Common:2; Rare:92 | ||||
| chr17:19648041-19648198 | Rare:32 | ||||
| chr17:19648608-19649092 | Common:3; Rare:175; Clinvar (benign):1 | ||||
| chr17:19977789-19977958 | Common:1; Rare:58 | ||||
| chr17:20009255-20009392 | Common:2; Rare:43 | ||||
| chr17:21214108-21214369 | Common:2; Rare:121 | ||||
| chr17:21214565-21214605 | Common:1; Rare:17 | ||||
| chr17:27293997-27294202 | Common:2; Rare:78 | ||||
| chr17:27294230-27294435 | Common:1; Rare:61 | ||||
| chr17:28331951-28332032 | Rare:22 | ||||
| chr17:28335361-28335847 | Common:1; Rare:116 | ||||
| chr17:28357289-28357699 | Common:11; Rare:185; Clinvar (pathogenic):1 | ||||
| chr17:28406189-28406263 | Rare:11 | ||||
| chr17:28571497-28571698 | Rare:47 |