| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:39437283-39437476 | Common:2; Rare:69 | ||||
| chr2:43226568-43226862 | Common:3; Rare:120 | ||||
| chr2:46616979-46617257 | Common:6; Rare:119 | ||||
| chr2:46915723-46915878 | Common:1; Rare:39; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:53786933-53787098 | Rare:68 | ||||
| chr2:53970755-53971147 | Common:11; Rare:141 | ||||
| chr2:55049642-55049867 | Rare:79 | ||||
| chr2:55050175-55050733 | Common:5; Rare:183 | ||||
| chr2:55232311-55232736 | Common:2; Rare:123 | ||||
| chr2:55519425-55519808 | Common:1; Rare:117 | ||||
| chr2:55544026-55544367 | Common:1; Rare:116 | ||||
| chr2:61017402-61017770 | Common:1; Rare:117; Clinvar:3; Clinvar (benign):2 | ||||
| chr2:61470702-61471014 | Rare:103 | ||||
| chr2:61471097-61471330 | Common:1; Rare:86 | ||||
| chr2:61888400-61888727 | Common:1; Rare:148 |