| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:106774005-106774435 | Common:3; Rare:109 | ||||
| chr12:106774458-106774731 | Common:2; Rare:79 | ||||
| chr12:106955431-106955981 | Common:5; Rare:205 | ||||
| chr12:106956651-106956795 | Rare:25 | ||||
| chr12:106987018-106987352 | Common:5; Rare:95 | ||||
| chr12:107093533-107093642 | Rare:36 | ||||
| chr12:107685612-107685959 | Common:2; Rare:111 | ||||
| chr12:107686018-107686111 | Rare:29 | ||||
| chr12:107760496-107760693 | Rare:54 | ||||
| chr12:107761042-107761374 | Common:6; Rare:126 | ||||
| chr12:108514939-108515377 | Common:1; Rare:132 | ||||
| chr12:108561071-108561448 | Common:4; Rare:109 | ||||
| chr12:108561478-108561595 | Rare:22 | ||||
| chr12:108562255-108562673 | Common:12; Rare:144; Clinvar:2; Clinvar (benign):4 | ||||
| chr12:108568079-108568166 | Rare:6 |