| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:171894212-171894355 | Rare:62; Clinvar:1 | ||||
| chr2:171922264-171922497 | Rare:91 | ||||
| chr2:171999798-171999972 | Common:1; Rare:71 | ||||
| chr2:172084623-172084809 | Rare:43 | ||||
| chr2:172086278-172086435 | Common:1; Rare:27 | ||||
| chr2:173965281-173965515 | Common:1; Rare:85 | ||||
| chr2:174248463-174248744 | Common:1; Rare:84 | ||||
| chr2:174395629-174395816 | Common:1; Rare:63 | ||||
| chr2:175168330-175168593 | Common:1; Rare:70 | ||||
| chr2:176002225-176002398 | Common:2; Rare:71 | ||||
| chr2:176269338-176269505 | Common:1; Rare:68 | ||||
| chr2:177212422-177212802 | Common:4; Rare:154 | ||||
| chr2:177264651-177264844 | Common:2; Rare:62 | ||||
| chr2:177392659-177393059 | Common:3; Rare:140; Clinvar:6; Clinvar (benign):4 | ||||
| chr2:177552768-177552826 | Rare:21 |