| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:171687574-171687810 | Rare:64 | ||||
| chr2:171687970-171688016 | Common:1; Rare:6 | ||||
| chr2:174395630-174395795 | Common:1; Rare:55 | ||||
| chr2:175181650-175181762 | Common:3; Rare:49 | ||||
| chr2:177263419-177263709 | Common:1; Rare:72 | ||||
| chr2:177264120-177264426 | Rare:85 | ||||
| chr2:177392669-177392795 | Rare:31; Clinvar:1 | ||||
| chr2:178451090-178451310 | Common:5; Rare:68; Clinvar:4; Clinvar (benign):3 | ||||
| chr2:182426606-182426878 | Common:1; Rare:49 | ||||
| chr2:186486087-186486331 | Common:3; Rare:75 | ||||
| chr2:186589896-186590069 | Rare:51 | ||||
| chr2:189441151-189441512 | Common:2; Rare:113 | ||||
| chr2:189783965-189784084 | Common:3; Rare:41; Clinvar (benign):1 | ||||
| chr2:189784325-189784518 | Common:3; Rare:65; Clinvar:7; Clinvar (benign):1 | ||||
| chr2:190343916-190343949 | Rare:5 |