| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:21437635-21437678 | Common:2; Rare:15 | ||||
| chr12:21501520-21501889 | Common:4; Rare:102 | ||||
| chr12:21657754-21657997 | Common:4; Rare:84; Clinvar:2; Clinvar (benign):1 | ||||
| chr12:22544466-22544774 | Common:2; Rare:69 | ||||
| chr12:22624998-22625239 | Common:1; Rare:116 | ||||
| chr12:23949655-23949905 | Common:5; Rare:41 | ||||
| chr12:24948411-24948630 | Common:1; Rare:41 | ||||
| chr12:24948986-24949219 | Common:1; Rare:52 | ||||
| chr12:25195151-25195304 | Common:1; Rare:45 | ||||
| chr12:26937936-26938053 | Common:3; Rare:34 | ||||
| chr12:26938268-26938544 | Common:3; Rare:104 | ||||
| chr12:27244029-27244325 | Common:2; Rare:96 | ||||
| chr12:27523984-27524235 | Rare:62 | ||||
| chr12:27710729-27710893 | Common:2; Rare:71 | ||||
| chr12:28190325-28190498 | Common:2; Rare:63 |