| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:176002807-176003214 | Common:6; Rare:144 | ||||
| chr2:176269150-176269530 | Common:6; Rare:445 | ||||
| chr2:176269718-176270139 | Common:5; Rare:214 | ||||
| chr2:177212099-177212861 | Common:35; Rare:1300 | ||||
| chr2:177212940-177213500 | Common:1; Rare:746 | ||||
| chr2:177263412-177263840 | Common:10; Rare:459 | ||||
| chr2:177263810-177264432 | Common:12; Rare:710 | ||||
| chr2:177264572-177265552 | Common:28; Rare:1009 | ||||
| chr2:177392340-177393391 | Common:24; Rare:832; Clinvar:24; Clinvar (benign):16 | ||||
| chr2:177552601-177553251 | Common:52; Rare:1426 | ||||
| chr2:177553226-177553710 | Common:3; Rare:121 | ||||
| chr2:177618600-177619240 | Common:40; Rare:806 | ||||
| chr2:177682780-177683337 | Common:12; Rare:148 | ||||
| chr2:177683485-177683586 | Common:2; Rare:24 | ||||
| chr2:177683493-177683606 | Common:2; Rare:26 |