| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:26937932-26938048 | Common:3; Rare:34 | ||||
| chr12:27244170-27244293 | Common:1; Rare:43 | ||||
| chr12:28190354-28190488 | Common:1; Rare:42 | ||||
| chr12:29381145-29381375 | Common:3; Rare:71 | ||||
| chr12:30754943-30755041 | Rare:40 | ||||
| chr12:31073760-31073872 | Common:6; Rare:42 | ||||
| chr12:31729019-31729288 | Common:1; Rare:81 | ||||
| chr12:31959269-31959458 | Common:2; Rare:61 | ||||
| chr12:32679050-32679342 | Common:2; Rare:111; Clinvar (benign):3 | ||||
| chr12:32755884-32755970 | Rare:32 | ||||
| chr12:42238193-42238471 | Rare:96 | ||||
| chr12:42326008-42326213 | Common:1; Rare:66 | ||||
| chr12:43758749-43759020 | Common:2; Rare:76; Clinvar:2 | ||||
| chr12:43806253-43806415 | Common:2; Rare:55 | ||||
| chr12:44876297-44876459 | Common:1; Rare:53 |