| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:43919785-43920071 | Common:1; Rare:58 | ||||
| chr2:43920509-43920677 | Common:1; Rare:29 | ||||
| chr2:43956927-43957080 | Common:3; Rare:34 | ||||
| chr2:44364041-44364269 | Common:2; Rare:45 | ||||
| chr2:44728868-44728882 | |||||
| chr2:44757809-44757933 | Rare:30 | ||||
| chr2:46360675-46360925 | Rare:76; Clinvar (benign):3 | ||||
| chr2:46587448-46587542 | Common:1; Rare:14 | ||||
| chr2:46587781-46587903 | Rare:28 | ||||
| chr2:46589137-46589298 | Rare:10 | ||||
| chr2:46589946-46590319 | Common:1; Rare:60 | ||||
| chr2:47162308-47162665 | Rare:59; Clinvar (benign):4 | ||||
| chr2:47171826-47172060 | Common:3; Rare:38 | ||||
| chr2:47795715-47795958 | Common:3; Rare:67; Clinvar:12; Clinvar (benign):9; Clinvar (pathogenic):1 | ||||
| chr2:47802572-47802871 | Common:2; Rare:78 |