| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:64682625-64682965 | Common:4; Rare:58 | ||||
| chr12:64682995-64683163 | Rare:24 | ||||
| chr12:65170480-65170553 | Common:1; Rare:30; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr12:65307019-65307255 | Common:1; Rare:38 | ||||
| chr12:65307983-65308015 | Rare:4 | ||||
| chr12:65308216-65308274 | Rare:5 | ||||
| chr12:65308647-65308826 | Rare:29; Clinvar:1 | ||||
| chr12:65335257-65335394 | Rare:24 | ||||
| chr12:65470312-65470520 | Common:2; Rare:49 | ||||
| chr12:65510649-65510885 | Rare:43 | ||||
| chr12:65510942-65511029 | Common:2; Rare:12 | ||||
| chr12:65511427-65511513 | Rare:17 | ||||
| chr12:65640507-65640781 | Common:1; Rare:61 | ||||
| chr12:65644114-65644256 | Common:1; Rare:22 | ||||
| chr12:65729056-65729205 | Common:1; Rare:41 |