| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:186485983-186486411 | Common:3; Rare:124 | ||||
| chr2:186589974-186590034 | Rare:12 | ||||
| chr2:187554133-187554161 | Rare:6 | ||||
| chr2:187554198-187554514 | Rare:64 | ||||
| chr2:189441094-189441501 | Common:2; Rare:118 | ||||
| chr2:189783921-189784133 | Common:4; Rare:74; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:189784281-189784512 | Common:3; Rare:76; Clinvar:7; Clinvar (benign):1 | ||||
| chr2:190180785-190181046 | Rare:81 | ||||
| chr2:190343795-190343955 | Rare:37 | ||||
| chr2:190343957-190344025 | Rare:12 | ||||
| chr2:190534651-190534972 | Common:2; Rare:102 | ||||
| chr2:190649420-190649574 | Common:1; Rare:46 | ||||
| chr2:190880621-190880859 | Common:4; Rare:81 | ||||
| chr2:191014129-191014363 | Common:2; Rare:83; Clinvar:2; Clinvar (benign):2 | ||||
| chr2:191245231-191245560 | Common:3; Rare:106 |