| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:188291577-188291762 | Common:3; Rare:49 | ||||
| chr2:188291812-188292066 | Common:3; Rare:84 | ||||
| chr2:188292692-188292869 | Common:1; Rare:44 | ||||
| chr2:188293000-188293064 | Rare:7 | ||||
| chr2:189441038-189441511 | Common:3; Rare:151 | ||||
| chr2:189580781-189580932 | Rare:42; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:189674464-189674749 | Common:1; Rare:65 | ||||
| chr2:189783921-189784123 | Common:4; Rare:70; Clinvar (benign):1 | ||||
| chr2:189784281-189784749 | Common:7; Rare:147; Clinvar:8; Clinvar (benign):3 | ||||
| chr2:190250469-190250651 | Rare:31 | ||||
| chr2:190319726-190320105 | Common:5; Rare:124; Clinvar (benign):5 | ||||
| chr2:190534638-190535024 | Common:5; Rare:119 | ||||
| chr2:190880644-190880890 | Common:4; Rare:85 | ||||
| chr2:191014124-191014357 | Common:2; Rare:84; Clinvar:2; Clinvar (benign):2 | ||||
| chr2:191020453-191020530 | Common:1; Rare:27 |