| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:38906161-38906229 | Rare:10 | ||||
| chr12:38906666-38907053 | Common:2; Rare:82 | ||||
| chr12:39442382-39442475 | Rare:18 | ||||
| chr12:39442567-39442915 | Common:1; Rare:76 | ||||
| chr12:39443037-39443512 | Common:2; Rare:138; Clinvar:8; Clinvar (benign):5 | ||||
| chr12:39443549-39443720 | Rare:40 | ||||
| chr12:39619451-39619610 | Common:1; Rare:46 | ||||
| chr12:39619827-39620242 | Common:1; Rare:70 | ||||
| chr12:40105453-40105474 | Rare:9 | ||||
| chr12:40105994-40106191 | Common:1; Rare:86 | ||||
| chr12:40224592-40224689 | Common:1; Rare:27 | ||||
| chr12:40224812-40225116 | Common:5; Rare:94; Clinvar:1; Clinvar (benign):1 | ||||
| chr12:40225657-40225685 | Rare:12 | ||||
| chr12:42144829-42145104 | Common:5; Rare:108 | ||||
| chr12:42237570-42237752 | Rare:58 |