| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:28190355-28190488 | Common:1; Rare:41 | ||||
| chr12:29381128-29381313 | Common:2; Rare:60 | ||||
| chr12:30695860-30695959 | Common:1; Rare:24 | ||||
| chr12:31073748-31073917 | Common:8; Rare:62 | ||||
| chr12:31074088-31074287 | Common:1; Rare:39 | ||||
| chr12:31728995-31729306 | Common:1; Rare:99 | ||||
| chr12:31959271-31959482 | Common:2; Rare:68 | ||||
| chr12:32679050-32679366 | Common:2; Rare:127; Clinvar:1; Clinvar (benign):4 | ||||
| chr12:32896760-32897043 | Common:3; Rare:91; Clinvar:4; Clinvar (benign):3 | ||||
| chr12:38905569-38905791 | Common:5; Rare:59 | ||||
| chr12:42326026-42326215 | Common:1; Rare:63 | ||||
| chr12:43758721-43759020 | Common:2; Rare:89; Clinvar:2 | ||||
| chr12:43806090-43806370 | Common:4; Rare:107 | ||||
| chr12:45216007-45216163 | Rare:49 | ||||
| chr12:45990504-45990959 | Common:2; Rare:148 |