| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:148020688-148021125 | Common:2; Rare:103; Clinvar (benign):2 | ||||
| chr2:148021366-148021561 | Rare:59 | ||||
| chr2:149330394-149330666 | Common:2; Rare:107 | ||||
| chr2:149587285-149587347 | Common:1; Rare:14 | ||||
| chr2:149587653-149587883 | Common:1; Rare:68; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:151828336-151828638 | Common:3; Rare:96 | ||||
| chr2:152175664-152176151 | Common:3; Rare:134 | ||||
| chr2:152717829-152718033 | Rare:82 | ||||
| chr2:152718481-152718647 | Rare:66 | ||||
| chr2:156435419-156435521 | Common:1; Rare:20 | ||||
| chr2:156436264-156436440 | Common:3; Rare:60 | ||||
| chr2:157257531-157257740 | Rare:37 | ||||
| chr2:158968465-158968721 | Rare:81 | ||||
| chr2:159286590-159286900 | Common:5; Rare:114 | ||||
| chr2:159615170-159615350 | Common:3; Rare:35 |