| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:30700586-30700842 | Common:2; Rare:37 | ||||
| chr12:37501958-37501991 | Rare:5 | ||||
| chr12:39239515-39239692 | Common:1; Rare:25 | ||||
| chr12:40310330-40310567 | Rare:68; Clinvar:6; Clinvar (pathogenic):2 | ||||
| chr12:40444063-40444525 | Common:4; Rare:152 | ||||
| chr12:40738930-40739126 | Rare:48 | ||||
| chr12:43885092-43885356 | Rare:51 | ||||
| chr12:43982660-43982856 | Rare:42 | ||||
| chr12:45727482-45727875 | Rare:150 | ||||
| chr12:46383131-46383451 | Common:1; Rare:122 | ||||
| chr12:46383965-46384029 | Rare:15 | ||||
| chr12:47085042-47085318 | Common:2; Rare:48 | ||||
| chr12:49060778-49060908 | Common:1; Rare:52 | ||||
| chr12:49138642-49138883 | Rare:39 | ||||
| chr12:49234492-49234711 | Common:1; Rare:64 |