| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:58558890-58559126 | Common:1; Rare:76 | ||||
| chr2:264007-264107 | Common:1; Rare:38 | ||||
| chr2:264558-264975 | Common:4; Rare:153 | ||||
| chr2:677369-677568 | Common:1; Rare:83 | ||||
| chr2:1744268-1744580 | Common:2; Rare:106 | ||||
| chr2:3377811-3378009 | Common:1; Rare:56 | ||||
| chr2:3379594-3379779 | Common:2; Rare:76 | ||||
| chr2:3519488-3519660 | Common:2; Rare:51 | ||||
| chr2:3558269-3558715 | Common:6; Rare:156 | ||||
| chr2:3575107-3575354 | Common:2; Rare:72; Clinvar:3; Clinvar (benign):5 | ||||
| chr2:9423404-9423756 | Rare:110 | ||||
| chr2:9555678-9555898 | Common:2; Rare:71 | ||||
| chr2:9630944-9631343 | Common:3; Rare:126 | ||||
| chr2:9843244-9843539 | Common:6; Rare:88 | ||||
| chr2:10689910-10690004 | Common:2; Rare:33 |