| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:164621340-164621700 | Common:3; Rare:93 | ||||
| chr2:164841192-164841460 | Rare:81 | ||||
| chr2:165953709-165954140 | Common:5; Rare:231; Clinvar:17; Clinvar (benign):4 | ||||
| chr2:168247360-168248060 | Common:12; Rare:381 | ||||
| chr2:169584070-169584642 | Common:3; Rare:247 | ||||
| chr2:169694389-169694571 | Common:9; Rare:88 | ||||
| chr2:169798708-169799056 | Common:1; Rare:154 | ||||
| chr2:169824838-169825057 | Common:4; Rare:65 | ||||
| chr2:169827322-169827505 | Rare:54 | ||||
| chr2:170928903-170929388 | Common:9; Rare:257 | ||||
| chr2:171160746-171161055 | Common:3; Rare:94 | ||||
| chr2:171433902-171434366 | Common:6; Rare:227 | ||||
| chr2:171434490-171434700 | Rare:65; Clinvar:1 | ||||
| chr2:171434654-171434801 | Rare:40 | ||||
| chr2:171687695-171687819 | Rare:42 |