| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:34961444-34961589 | Common:1; Rare:71 | ||||
| chr17:34980357-34980618 | Common:4; Rare:75 | ||||
| chr17:35119609-35120013 | Common:1; Rare:139; Clinvar:6; Clinvar (benign):10; Clinvar (pathogenic):1 | ||||
| chr17:35578539-35578727 | Common:2; Rare:48; Clinvar (benign):1 | ||||
| chr17:35587148-35587519 | Common:1; Rare:106 | ||||
| chr17:35809296-35809533 | Rare:96 | ||||
| chr17:35930737-35930854 | Rare:43 | ||||
| chr17:36486476-36486724 | Common:3; Rare:88 | ||||
| chr17:36534191-36534335 | Rare:36 | ||||
| chr17:36534777-36535069 | Common:3; Rare:118 | ||||
| chr17:36544749-36544971 | Common:3; Rare:75 | ||||
| chr17:36601483-36601616 | Rare:42 | ||||
| chr17:36948830-36949139 | Common:2; Rare:110 | ||||
| chr17:37359000-37359593 | Common:1; Rare:171 | ||||
| chr17:37406721-37406936 | Rare:86 |