| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:57490333-57490615 | Rare:65; Clinvar:4; Clinvar (benign):3 | ||||
| chr12:57936130-57936260 | Common:2; Rare:41 | ||||
| chr12:62602723-62602852 | Rare:56 | ||||
| chr12:64665527-64665745 | Rare:41 | ||||
| chr12:67991303-67991448 | Common:1; Rare:25 | ||||
| chr12:68163589-68163747 | Rare:19 | ||||
| chr12:71755388-71755607 | Rare:41 | ||||
| chr12:74538615-74538680 | Rare:25 | ||||
| chr12:74539088-74539277 | Rare:39 | ||||
| chr12:74540895-74541301 | Common:3; Rare:86 | ||||
| chr12:75482798-75482950 | Rare:26 | ||||
| chr12:89709856-89710184 | Common:3; Rare:107 | ||||
| chr12:89710534-89710755 | Common:1; Rare:62 | ||||
| chr12:89927187-89927562 | Common:1; Rare:51 | ||||
| chr12:92124279-92124550 | Common:3; Rare:35 |