| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:16491806-16491915 | Rare:22 | ||||
| chr17:16492053-16492383 | Common:3; Rare:111 | ||||
| chr17:16569084-16569220 | Rare:51 | ||||
| chr17:16653303-16653421 | Common:2; Rare:24 | ||||
| chr17:16653559-16653607 | Rare:17 | ||||
| chr17:16653611-16653641 | Rare:10 | ||||
| chr17:16653743-16654082 | Rare:87 | ||||
| chr17:17042210-17042563 | Common:20; Rare:125 | ||||
| chr17:17206153-17206594 | Common:4; Rare:167 | ||||
| chr17:17237098-17237198 | Common:1; Rare:43; Clinvar:1; Clinvar (benign):3 | ||||
| chr17:17237314-17237763 | Common:7; Rare:122 | ||||
| chr17:17280365-17280480 | Rare:25 | ||||
| chr17:17280587-17281001 | Common:5; Rare:158 | ||||
| chr17:17281135-17281497 | Common:1; Rare:123 | ||||
| chr17:17281614-17281691 | Rare:9 |