| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:183038009-183038077 | Rare:19 | ||||
| chr2:183038090-183038207 | Rare:36 | ||||
| chr2:183038257-183038532 | Common:3; Rare:79 | ||||
| chr2:186486076-186486445 | Common:3; Rare:118 | ||||
| chr2:186505455-186505840 | Rare:92 | ||||
| chr2:186589685-186589875 | Rare:45 | ||||
| chr2:186589878-186590130 | Rare:78 | ||||
| chr2:186590237-186590341 | Rare:32 | ||||
| chr2:187553745-187554190 | Rare:75 | ||||
| chr2:187554196-187554548 | Rare:70 | ||||
| chr2:188291565-188292066 | Common:6; Rare:143 | ||||
| chr2:188292692-188292941 | Common:1; Rare:59 | ||||
| chr2:188292969-188293087 | Rare:17 | ||||
| chr2:189179503-189179659 | Rare:50; Clinvar:4; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr2:189441065-189441552 | Common:2; Rare:166 |