| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:55693338-55693479 | Rare:34 | ||||
| chr2:55693749-55694009 | Common:1; Rare:93; Clinvar (benign):2 | ||||
| chr2:58046376-58046460 | Common:1; Rare:26 | ||||
| chr2:58046527-58046895 | Common:2; Rare:107 | ||||
| chr2:58046904-58047275 | Common:3; Rare:122 | ||||
| chr2:58240926-58241163 | Rare:74 | ||||
| chr2:58241225-58241495 | Common:1; Rare:130; Clinvar:5; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr2:60756076-60756404 | Common:1; Rare:108 | ||||
| chr2:60880965-60881695 | Common:3; Rare:227 | ||||
| chr2:60881936-60882190 | Common:1; Rare:64 | ||||
| chr2:61017140-61017281 | Common:3; Rare:38 | ||||
| chr2:61017388-61017769 | Common:1; Rare:123; Clinvar:3; Clinvar (benign):2 | ||||
| chr2:61018026-61018379 | Common:1; Rare:114 | ||||
| chr2:61065675-61066012 | Common:3; Rare:112 | ||||
| chr2:61144833-61145206 | Common:3; Rare:113 |