| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:122079085-122079199 | Rare:19 | ||||
| chr12:122182995-122183258 | Common:1; Rare:88 | ||||
| chr12:122203392-122203483 | Rare:39 | ||||
| chr12:122203596-122203758 | Common:1; Rare:54 | ||||
| chr12:122225224-122225496 | Common:1; Rare:87 | ||||
| chr12:122225575-122225778 | Common:1; Rare:52 | ||||
| chr12:122225792-122225882 | Rare:30 | ||||
| chr12:122225910-122226623 | Common:3; Rare:334; Clinvar:3; Clinvar (benign):1 | ||||
| chr12:122265937-122266106 | Common:1; Rare:46 | ||||
| chr12:122266292-122266657 | Common:2; Rare:125 | ||||
| chr12:122267015-122267079 | Rare:6 | ||||
| chr12:122279936-122279987 | Rare:6 | ||||
| chr12:122399423-122399688 | Common:1; Rare:48 | ||||
| chr12:122399697-122399756 | Rare:8 | ||||
| chr12:122399982-122400152 | Rare:35 |