| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:18087803-18087985 | Rare:45 | ||||
| chr17:18183013-18183071 | Rare:19 | ||||
| chr17:18183693-18183925 | Rare:105 | ||||
| chr17:18225374-18225684 | Common:4; Rare:105 | ||||
| chr17:18260446-18260668 | Rare:66 | ||||
| chr17:18314921-18315326 | Common:1; Rare:114 | ||||
| chr17:18363399-18363690 | Common:4; Rare:99 | ||||
| chr17:18682206-18682482 | Common:9; Rare:27 | ||||
| chr17:18697973-18698028 | Common:1; Rare:14 | ||||
| chr17:18781075-18781318 | Common:5; Rare:68 | ||||
| chr17:18856140-18856362 | Common:1; Rare:38 | ||||
| chr17:18857926-18858231 | Common:6; Rare:76 | ||||
| chr17:19362565-19362804 | Common:2; Rare:110; Clinvar:1; Clinvar (benign):2 | ||||
| chr17:19377638-19377768 | Common:1; Rare:36 | ||||
| chr17:19377880-19378029 | Common:1; Rare:38 |