| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:15688350-15688565 | Common:1; Rare:36 | ||||
| chr12:15788361-15788498 | Common:1; Rare:36 | ||||
| chr12:15911882-15912137 | Common:4; Rare:48 | ||||
| chr12:16021812-16022054 | Common:1; Rare:40 | ||||
| chr12:16030907-16031210 | Rare:47 | ||||
| chr12:18383232-18383382 | Rare:32 | ||||
| chr12:18951309-18951482 | Common:2; Rare:35 | ||||
| chr12:19066471-19066698 | Rare:34 | ||||
| chr12:19971369-19971751 | Common:2; Rare:78 | ||||
| chr12:21645000-21645240 | Common:3; Rare:47 | ||||
| chr12:21773287-21773557 | Common:1; Rare:53; Clinvar:3; Clinvar (benign):4 | ||||
| chr12:21774003-21774051 | Rare:7 | ||||
| chr12:21819168-21819493 | Common:3; Rare:54 | ||||
| chr12:21819683-21820015 | Common:3; Rare:57 | ||||
| chr12:21820643-21820693 | Rare:8 |