| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:51238648-51238914 | Common:8; Rare:115 | ||||
| chr12:51270264-51270431 | Common:3; Rare:48 | ||||
| chr12:51391377-51391466 | Common:1; Rare:22 | ||||
| chr12:51391610-51391737 | Common:1; Rare:39 | ||||
| chr12:51912241-51912450 | Common:2; Rare:53; Clinvar (benign):1 | ||||
| chr12:52051097-52051449 | Common:1; Rare:123 | ||||
| chr12:52948830-52949171 | Common:2; Rare:88; Clinvar:1 | ||||
| chr12:52949768-52950044 | Rare:59 | ||||
| chr12:53006117-53006489 | Common:4; Rare:134 | ||||
| chr12:53079335-53079423 | Rare:39 | ||||
| chr12:53097929-53098229 | Common:1; Rare:80 | ||||
| chr12:53251992-53252217 | Common:3; Rare:87 | ||||
| chr12:53268080-53268320 | Common:3; Rare:61 | ||||
| chr12:53299820-53299972 | Rare:67 | ||||
| chr12:53380088-53380286 | Common:4; Rare:82 |