| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:201132598-201132782 | Rare:24 | ||||
| chr2:201182948-201183163 | Common:2; Rare:31; Clinvar (benign):3 | ||||
| chr2:201233321-201233579 | Common:1; Rare:42 | ||||
| chr2:201257950-201258119 | Common:1; Rare:30 | ||||
| chr2:201258351-201258487 | Rare:37 | ||||
| chr2:201260425-201260598 | Rare:37 | ||||
| chr2:201451308-201451840 | Common:2; Rare:137 | ||||
| chr2:201642593-201642827 | Common:1; Rare:98; Clinvar (benign):1 | ||||
| chr2:201780735-201781010 | Common:3; Rare:75; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:202238474-202238891 | Common:1; Rare:109; Clinvar:1 | ||||
| chr2:202265137-202265246 | Common:1; Rare:17 | ||||
| chr2:202265603-202265868 | Rare:90 | ||||
| chr2:202377009-202377350 | Common:2; Rare:80; Clinvar:1; Clinvar (benign):3 | ||||
| chr2:202634743-202635029 | Common:6; Rare:100 | ||||
| chr2:202635845-202636256 | Common:5; Rare:114 |