| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:15699616-15699773 | Common:1; Rare:45 | ||||
| chr17:15732170-15732289 | Common:1; Rare:23 | ||||
| chr17:15999591-15999748 | Common:1; Rare:86; Clinvar:2; Clinvar (benign):3 | ||||
| chr17:16039761-16039879 | Common:1; Rare:28 | ||||
| chr17:16215429-16215474 | Rare:11 | ||||
| chr17:16215538-16215650 | Common:1; Rare:49 | ||||
| chr17:16217115-16217268 | Rare:57; Clinvar:2 | ||||
| chr17:16380656-16380829 | Common:2; Rare:42 | ||||
| chr17:16380998-16381451 | Common:4; Rare:191 | ||||
| chr17:16569140-16569249 | Rare:44 | ||||
| chr17:16653615-16653758 | Common:2; Rare:39 | ||||
| chr17:16653785-16653807 | Rare:7 | ||||
| chr17:16653819-16653948 | Rare:37 | ||||
| chr17:16689914-16690734 | Common:8; Rare:248 | ||||
| chr17:17237101-17237727 | Common:8; Rare:175; Clinvar:1; Clinvar (benign):3 |