| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:188292920-188293360 | Common:1; Rare:87 | ||||
| chr2:188293905-188294305 | Common:5; Rare:69 | ||||
| chr2:189179745-189179880 | Rare:14; Clinvar:1 | ||||
| chr2:189441006-189441687 | Common:4; Rare:223 | ||||
| chr2:189580600-189581160 | Common:3; Rare:152; Clinvar:2; Clinvar (benign):2 | ||||
| chr2:189762220-189762660 | Common:1; Rare:98 | ||||
| chr2:189762721-189762852 | Rare:44 | ||||
| chr2:189783818-189784115 | Common:4; Rare:85; Clinvar (benign):1 | ||||
| chr2:189784234-189784567 | Common:4; Rare:115; Clinvar:8; Clinvar (benign):3 | ||||
| chr2:189784684-189784791 | Common:2; Rare:36 | ||||
| chr2:190180121-190180521 | Common:4; Rare:119 | ||||
| chr2:190180609-190181030 | Rare:201 | ||||
| chr2:190319727-190320133 | Common:5; Rare:133; Clinvar (benign):5 | ||||
| chr2:190534310-190534960 | Common:10; Rare:201 | ||||
| chr2:190648684-190648906 | Common:1; Rare:82 |