| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:16215407-16215967 | Common:8; Rare:212 | ||||
| chr17:16217046-16217458 | Rare:125; Clinvar:3; Clinvar (pathogenic):1 | ||||
| chr17:16352781-16353053 | Common:1; Rare:75 | ||||
| chr17:16353111-16353189 | Rare:29 | ||||
| chr17:16353191-16353292 | Rare:31 | ||||
| chr17:16353341-16353678 | Common:1; Rare:123 | ||||
| chr17:16380612-16380801 | Common:2; Rare:42 | ||||
| chr17:16380979-16381429 | Common:4; Rare:188 | ||||
| chr17:16419204-16419349 | Rare:36 | ||||
| chr17:16653300-16653433 | Common:2; Rare:26 | ||||
| chr17:16653465-16653671 | Common:1; Rare:63 | ||||
| chr17:16653741-16654079 | Rare:87 | ||||
| chr17:17042171-17042730 | Common:22; Rare:173 | ||||
| chr17:17043186-17043250 | Common:1; Rare:14 | ||||
| chr17:17205910-17206404 | Common:1; Rare:194 |