| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6774781-6775181 | Common:3; Rare:196 | ||||
| chr12:6775620-6775900 | Common:2; Rare:57 | ||||
| chr12:6778880-6779370 | Common:7; Rare:129 | ||||
| chr12:6792570-6792950 | Common:3; Rare:94 | ||||
| chr12:6792960-6793410 | Common:1; Rare:84 | ||||
| chr12:6852880-6852988 | Rare:24 | ||||
| chr12:6871490-6871890 | Common:6; Rare:167 | ||||
| chr12:6890959-6891559 | Common:16; Rare:627 | ||||
| chr12:6891477-6891877 | Common:2; Rare:74 | ||||
| chr12:6900013-6900236 | Common:4; Rare:38 | ||||
| chr12:6925673-6926117 | Common:4; Rare:102 | ||||
| chr12:6929429-6930287 | Common:5; Rare:161 | ||||
| chr12:6933978-6934260 | Rare:76 | ||||
| chr12:6945178-6945891 | Common:4; Rare:193; Clinvar:2; Clinvar (benign):3 | ||||
| chr12:6949330-6950441 | Common:18; Rare:259 |