| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:40224889-40225108 | Common:3; Rare:68; Clinvar:1; Clinvar (benign):1 | ||||
| chr12:42326083-42326220 | Common:1; Rare:40 | ||||
| chr12:42483942-42484174 | Common:1; Rare:29 | ||||
| chr12:42484265-42484533 | Common:3; Rare:52 | ||||
| chr12:43758752-43759024 | Common:2; Rare:76; Clinvar:2 | ||||
| chr12:43806307-43806397 | Common:1; Rare:22 | ||||
| chr12:45216014-45216122 | Rare:34 | ||||
| chr12:45729559-45729741 | Rare:56 | ||||
| chr12:45990521-45990919 | Common:2; Rare:129 | ||||
| chr12:46268555-46268743 | Common:1; Rare:34 | ||||
| chr12:46372643-46372954 | Rare:131 | ||||
| chr12:47079508-47079644 | Common:1; Rare:27 | ||||
| chr12:47705960-47706126 | Rare:71 | ||||
| chr12:48716649-48717008 | Common:4; Rare:107 | ||||
| chr12:48839847-48840057 | Rare:51 |