| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:104958237-104958430 | Common:3; Rare:58 | ||||
| chr12:104958670-104958742 | Rare:10 | ||||
| chr12:104986220-104986355 | Common:2; Rare:46 | ||||
| chr12:105107612-105107818 | Common:1; Rare:96; Clinvar:1 | ||||
| chr12:105236025-105236279 | Common:2; Rare:106 | ||||
| chr12:106774085-106774381 | Common:3; Rare:78 | ||||
| chr12:106774533-106774692 | Rare:47 | ||||
| chr12:106955625-106955920 | Rare:109 | ||||
| chr12:106987040-106987315 | Common:5; Rare:77 | ||||
| chr12:107093232-107093619 | Common:2; Rare:115 | ||||
| chr12:107685638-107685895 | Common:2; Rare:84 | ||||
| chr12:108339070-108339121 | Rare:5 | ||||
| chr12:108515047-108515313 | Common:1; Rare:80 | ||||
| chr12:108562388-108562691 | Common:9; Rare:125; Clinvar:2; Clinvar (benign):6 | ||||
| chr12:108633773-108633992 | Rare:41 |