| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:189674220-189674843 | Common:8; Rare:274 | ||||
| chr2:189762370-189763151 | Common:3; Rare:432 | ||||
| chr2:189763155-189763271 | Rare:24 | ||||
| chr2:189783927-189784183 | Common:12; Rare:194; Clinvar:2; Clinvar (benign):4 | ||||
| chr2:189784230-189784575 | Common:12; Rare:334; Clinvar:24; Clinvar (benign):8 | ||||
| chr2:190319690-190320004 | Common:9; Rare:189; Clinvar (benign):11 | ||||
| chr2:190343461-190343607 | Rare:33 | ||||
| chr2:190407670-190408450 | Common:9; Rare:328 | ||||
| chr2:190408670-190409160 | Common:3; Rare:127 | ||||
| chr2:190469914-190470073 | Rare:23 | ||||
| chr2:190534292-190535042 | Common:24; Rare:505 | ||||
| chr2:190648492-190649133 | Common:13; Rare:403 | ||||
| chr2:190880552-190881020 | Common:14; Rare:441 | ||||
| chr2:191013016-191013770 | Common:3; Rare:176; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:191013996-191014431 | Common:7; Rare:322; Clinvar:6; Clinvar (benign):7 |