| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:55519349-55519799 | Common:1; Rare:146 | ||||
| chr2:55616850-55617059 | Common:1; Rare:72 | ||||
| chr2:55617484-55618013 | Common:6; Rare:194 | ||||
| chr2:55618834-55618889 | Rare:21 | ||||
| chr2:55693742-55693991 | Common:1; Rare:90; Clinvar (benign):2 | ||||
| chr2:58240900-58240948 | Rare:16 | ||||
| chr2:58240952-58241542 | Common:1; Rare:235; Clinvar:5; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr2:60550836-60551018 | Rare:43 | ||||
| chr2:60552697-60553022 | Common:4; Rare:82 | ||||
| chr2:60553623-60553723 | Rare:20 | ||||
| chr2:60554019-60554237 | Common:1; Rare:69 | ||||
| chr2:60756099-60756364 | Rare:89 | ||||
| chr2:60880771-60881223 | Common:2; Rare:119 | ||||
| chr2:60881362-60881751 | Common:3; Rare:133 | ||||
| chr2:61017111-61017264 | Common:2; Rare:42 |