| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:18781518-18781663 | Common:3; Rare:32 | ||||
| chr17:18856069-18856401 | Common:1; Rare:68 | ||||
| chr17:18857903-18858239 | Common:6; Rare:81 | ||||
| chr17:18858345-18858441 | Rare:20 | ||||
| chr17:18858582-18858634 | Rare:9 | ||||
| chr17:19004119-19004344 | Rare:51 | ||||
| chr17:19004447-19004555 | Common:1; Rare:15 | ||||
| chr17:19004673-19004858 | Rare:52 | ||||
| chr17:19362302-19362416 | Rare:14 | ||||
| chr17:19362525-19362906 | Common:3; Rare:153; Clinvar:1; Clinvar (benign):3 | ||||
| chr17:19362916-19363122 | Common:2; Rare:46 | ||||
| chr17:19377603-19377701 | Common:1; Rare:27 | ||||
| chr17:19377754-19377780 | Common:1; Rare:5 | ||||
| chr17:19377795-19378085 | Common:3; Rare:66 | ||||
| chr17:19378108-19378271 | Rare:36 |