| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:55519404-55519875 | Common:2; Rare:156 | ||||
| chr2:55618847-55618881 | Rare:11 | ||||
| chr2:55693808-55694042 | Common:1; Rare:73; Clinvar (benign):2 | ||||
| chr2:58046612-58046861 | Common:1; Rare:77 | ||||
| chr2:58047103-58047142 | Rare:11 | ||||
| chr2:58047206-58047304 | Rare:33 | ||||
| chr2:60881315-60881664 | Common:2; Rare:134 | ||||
| chr2:61017156-61017756 | Common:5; Rare:177; Clinvar:2; Clinvar (benign):2 | ||||
| chr2:61144901-61145184 | Common:3; Rare:94 | ||||
| chr2:61177158-61177472 | Common:6; Rare:126 | ||||
| chr2:61470651-61470985 | Rare:112 | ||||
| chr2:61471131-61471387 | Common:2; Rare:99 | ||||
| chr2:61536638-61536767 | Rare:41 | ||||
| chr2:61853986-61854228 | Common:2; Rare:99; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:61888494-61888748 | Common:2; Rare:105 |