| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:35063633-35063838 | Rare:35 | ||||
| chr17:35242931-35243081 | Rare:48 | ||||
| chr17:35373611-35373839 | Common:4; Rare:44 | ||||
| chr17:35578486-35578713 | Common:1; Rare:59; Clinvar:1; Clinvar (benign):1 | ||||
| chr17:36001451-36001607 | Common:1; Rare:41 | ||||
| chr17:36001995-36002279 | Common:5; Rare:51 | ||||
| chr17:36090133-36090244 | Common:1; Rare:21 | ||||
| chr17:36534799-36535042 | Common:3; Rare:104 | ||||
| chr17:36544775-36545057 | Common:5; Rare:88 | ||||
| chr17:36601491-36601630 | Rare:42 | ||||
| chr17:37406721-37406936 | Rare:86 | ||||
| chr17:37489695-37489941 | Common:1; Rare:100 | ||||
| chr17:37609309-37609561 | Common:1; Rare:103 | ||||
| chr17:37745056-37745201 | Rare:37; Clinvar (benign):2 | ||||
| chr17:37745291-37745336 | Rare:10 |