| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:203239198-203239379 | Rare:61 | ||||
| chr2:203328189-203328512 | Common:2; Rare:117 | ||||
| chr2:203328537-203328616 | Rare:13 | ||||
| chr2:203535175-203535279 | Rare:23 | ||||
| chr2:203535281-203535533 | Common:2; Rare:113 | ||||
| chr2:206085838-206085995 | Common:1; Rare:36 | ||||
| chr2:206159342-206159932 | Common:4; Rare:160; Clinvar (benign):1 | ||||
| chr2:206162579-206162901 | Common:1; Rare:81 | ||||
| chr2:206765288-206765725 | Common:3; Rare:117; Clinvar:5; Clinvar (benign):6 | ||||
| chr2:207165758-207166342 | Common:2; Rare:151 | ||||
| chr2:207166833-207166984 | Common:2; Rare:68 | ||||
| chr2:207529771-207530129 | Common:3; Rare:98 | ||||
| chr2:207625190-207625539 | Common:1; Rare:97 | ||||
| chr2:207750056-207750379 | Common:4; Rare:43 | ||||
| chr2:208254069-208254253 | Common:1; Rare:33 |