| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:190408130-190408465 | Common:3; Rare:91 | ||||
| chr2:190469310-190469499 | Common:1; Rare:31 | ||||
| chr2:190489564-190489859 | Common:2; Rare:60 | ||||
| chr2:190534471-190534552 | Common:3; Rare:25 | ||||
| chr2:190534651-190534882 | Common:1; Rare:73 | ||||
| chr2:190648413-190648648 | Common:6; Rare:65 | ||||
| chr2:190648674-190649252 | Common:4; Rare:193 | ||||
| chr2:190880643-190880859 | Common:4; Rare:75 | ||||
| chr2:190881100-190881321 | Common:1; Rare:88 | ||||
| chr2:191014115-191014381 | Common:2; Rare:102; Clinvar:2; Clinvar (benign):2 | ||||
| chr2:191245231-191245570 | Common:3; Rare:108 | ||||
| chr2:191246144-191246314 | Common:1; Rare:50 | ||||
| chr2:191677828-191678201 | Common:4; Rare:106 | ||||
| chr2:191846722-191847104 | Rare:107 | ||||
| chr2:191847106-191847300 | Rare:31 |