| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:51026321-51026515 | Common:3; Rare:85; Clinvar:1; Clinvar (benign):2 | ||||
| chr12:51048077-51048369 | Common:2; Rare:103 | ||||
| chr12:51172780-51172982 | Common:2; Rare:47 | ||||
| chr12:51238648-51238918 | Common:8; Rare:115 | ||||
| chr12:51239121-51239326 | Common:2; Rare:59 | ||||
| chr12:51391613-51391736 | Common:1; Rare:39 | ||||
| chr12:51951456-51951744 | Common:4; Rare:111 | ||||
| chr12:52051175-52051480 | Common:1; Rare:96 | ||||
| chr12:52069942-52070033 | Common:1; Rare:31 | ||||
| chr12:52905029-52905223 | Common:2; Rare:54 | ||||
| chr12:53006117-53006489 | Common:4; Rare:134 | ||||
| chr12:53079145-53079568 | Common:3; Rare:122 | ||||
| chr12:53097343-53097682 | Common:1; Rare:69 | ||||
| chr12:53098032-53098190 | Common:1; Rare:43 | ||||
| chr12:53180436-53180573 | Rare:51 |