| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:44829532-44829726 | Common:1; Rare:55 | ||||
| chr17:44829780-44829860 | Common:1; Rare:14 | ||||
| chr17:44829904-44830332 | Common:2; Rare:155 | ||||
| chr17:44899016-44899189 | Common:1; Rare:46 | ||||
| chr17:44899347-44899811 | Common:3; Rare:133; Clinvar:3; Clinvar (benign):1 | ||||
| chr17:44899937-44900067 | Common:2; Rare:28 | ||||
| chr17:44947181-44947381 | Common:1; Rare:36 | ||||
| chr17:44947481-44947986 | Common:2; Rare:130 | ||||
| chr17:44968267-44968587 | Rare:85 | ||||
| chr17:45051252-45051728 | Common:2; Rare:151 | ||||
| chr17:45051892-45052123 | Common:3; Rare:12 | ||||
| chr17:45060604-45060639 | Rare:4 | ||||
| chr17:45060968-45061391 | Common:2; Rare:126 | ||||
| chr17:45061500-45061694 | Rare:41 | ||||
| chr17:45132482-45132749 | Common:3; Rare:86 |