| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:164955178-164955201 | Rare:6 | ||||
| chr2:165469561-165469705 | Rare:27 | ||||
| chr2:165793585-165794504 | Common:8; Rare:213; Clinvar:6; Clinvar (benign):1 | ||||
| chr2:165794564-165794601 | Rare:5 | ||||
| chr2:165794647-165794794 | Common:1; Rare:25 | ||||
| chr2:165953686-165953943 | Common:2; Rare:111; Clinvar:10; Clinvar (benign):2 | ||||
| chr2:165954119-165954287 | Common:1; Rare:47 | ||||
| chr2:166375702-166375752 | Rare:11 | ||||
| chr2:166375907-166376174 | Common:4; Rare:85; Clinvar:1; Clinvar (benign):5 | ||||
| chr2:166376483-166376538 | Rare:6 | ||||
| chr2:168455765-168455934 | Common:5; Rare:25 | ||||
| chr2:168456078-168456350 | Rare:92 | ||||
| chr2:168456563-168456824 | Rare:87 | ||||
| chr2:168802397-168802705 | Common:2; Rare:71 | ||||
| chr2:168803143-168803218 | Common:1; Rare:15 |