| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:189674161-189674758 | Common:4; Rare:119 | ||||
| chr2:189783870-189784123 | Common:4; Rare:82; Clinvar (benign):1 | ||||
| chr2:189784260-189784560 | Common:4; Rare:105; Clinvar:8; Clinvar (benign):3 | ||||
| chr2:189857292-189857409 | Rare:19 | ||||
| chr2:189879419-189879472 | Rare:16 | ||||
| chr2:189879518-189879670 | Rare:36 | ||||
| chr2:190137637-190137820 | Rare:29 | ||||
| chr2:190281039-190281248 | Rare:22 | ||||
| chr2:190319714-190319983 | Common:5; Rare:100; Clinvar (benign):5 | ||||
| chr2:190319984-190320044 | Rare:12 | ||||
| chr2:190343554-190343924 | Common:2; Rare:99 | ||||
| chr2:190534257-190534551 | Common:8; Rare:79 | ||||
| chr2:190534651-190534907 | Common:1; Rare:78 | ||||
| chr2:190648469-190648548 | Common:5; Rare:35 | ||||
| chr2:190648688-190649205 | Common:4; Rare:174 |