| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:44350266-44350794 | Common:1; Rare:184; Clinvar:10; Clinvar (benign):6 | ||||
| chr17:44503367-44503713 | Rare:134 | ||||
| chr17:44557085-44557349 | Common:1; Rare:47 | ||||
| chr17:44899375-44899774 | Common:3; Rare:126; Clinvar:3; Clinvar (benign):1 | ||||
| chr17:44947700-44947897 | Common:1; Rare:54 | ||||
| chr17:45060958-45061354 | Common:3; Rare:110 | ||||
| chr17:45148165-45148615 | Common:1; Rare:158 | ||||
| chr17:45317008-45317166 | Common:3; Rare:49 | ||||
| chr17:45490713-45490921 | Common:6; Rare:68 | ||||
| chr17:46193411-46193595 | Common:3; Rare:49 | ||||
| chr17:46225353-46225489 | Common:2; Rare:37 | ||||
| chr17:46922858-46923193 | Common:4; Rare:96; Clinvar:2; Clinvar (benign):7 | ||||
| chr17:47189250-47189569 | Rare:81 | ||||
| chr17:47323864-47323987 | Common:1; Rare:41 | ||||
| chr17:47821757-47821915 | Common:1; Rare:33 |