| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:162073975-162074181 | Rare:56 | ||||
| chr2:162318360-162319320 | Common:4; Rare:194 | ||||
| chr2:162343840-162344232 | Common:2; Rare:131 | ||||
| chr2:162344303-162344455 | Common:1; Rare:51 | ||||
| chr2:165794641-165794866 | Common:1; Rare:40 | ||||
| chr2:165953724-165953968 | Common:2; Rare:98; Clinvar:6; Clinvar (benign):2 | ||||
| chr2:165954078-165954310 | Common:2; Rare:61 | ||||
| chr2:168455917-168456324 | Common:2; Rare:120 | ||||
| chr2:168456561-168456793 | Rare:81 | ||||
| chr2:168890331-168890570 | Common:2; Rare:61 | ||||
| chr2:169479341-169479799 | Common:5; Rare:155; Clinvar (benign):2 | ||||
| chr2:169573735-169574036 | Common:2; Rare:82 | ||||
| chr2:169584268-169584428 | Rare:67 | ||||
| chr2:169584562-169584839 | Rare:75 | ||||
| chr2:169694373-169694647 | Common:6; Rare:86 |