| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:174597714-174597968 | Rare:31 | ||||
| chr2:174634516-174634666 | Rare:34 | ||||
| chr2:177216699-177216947 | Rare:81 | ||||
| chr2:177264646-177264893 | Common:2; Rare:77 | ||||
| chr2:177392657-177392781 | Common:1; Rare:30; Clinvar:1 | ||||
| chr2:178451098-178451378 | Common:5; Rare:82; Clinvar:3; Clinvar (benign):3 | ||||
| chr2:180980857-180980959 | Rare:24 | ||||
| chr2:181891650-181891964 | Common:4; Rare:125 | ||||
| chr2:182717652-182717956 | Common:2; Rare:59 | ||||
| chr2:186485998-186486364 | Common:3; Rare:108 | ||||
| chr2:189783937-189784140 | Common:5; Rare:73; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:189784331-189784513 | Common:1; Rare:59; Clinvar:6 | ||||
| chr2:190319740-190319972 | Common:5; Rare:83; Clinvar (benign):5 | ||||
| chr2:190343944-190344038 | Rare:20 | ||||
| chr2:190880590-190880862 | Common:4; Rare:97 |