| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:27710738-27710893 | Common:2; Rare:70 | ||||
| chr12:28190201-28190500 | Common:3; Rare:92 | ||||
| chr12:29381136-29381342 | Common:2; Rare:66 | ||||
| chr12:31073732-31073872 | Common:7; Rare:49 | ||||
| chr12:31326084-31326435 | Common:4; Rare:119 | ||||
| chr12:31728993-31729292 | Common:1; Rare:93 | ||||
| chr12:31959284-31959482 | Common:2; Rare:62 | ||||
| chr12:32679107-32679393 | Common:1; Rare:118; Clinvar:1; Clinvar (benign):4 | ||||
| chr12:38905530-38905701 | Common:3; Rare:48 | ||||
| chr12:38906267-38906567 | Common:2; Rare:62 | ||||
| chr12:39619785-39620101 | Common:2; Rare:52 | ||||
| chr12:40692317-40692571 | Common:1; Rare:81 | ||||
| chr12:41437571-41437787 | Rare:48 | ||||
| chr12:42326023-42326212 | Common:1; Rare:63 | ||||
| chr12:43758749-43759007 | Common:2; Rare:72; Clinvar:2 |