| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:21501556-21501900 | Common:4; Rare:88 | ||||
| chr12:21657754-21657997 | Common:4; Rare:84; Clinvar:2; Clinvar (benign):1 | ||||
| chr12:21774662-21775066 | Rare:73 | ||||
| chr12:21941219-21941370 | Rare:35 | ||||
| chr12:22544154-22544321 | Common:1; Rare:86 | ||||
| chr12:22544456-22544759 | Common:2; Rare:68 | ||||
| chr12:22625023-22625257 | Rare:119 | ||||
| chr12:23949579-23949774 | Common:2; Rare:45 | ||||
| chr12:25052526-25052729 | Common:2; Rare:47 | ||||
| chr12:25195142-25195308 | Common:1; Rare:50 | ||||
| chr12:26833140-26833469 | Common:2; Rare:99 | ||||
| chr12:26937936-26938708 | Common:12; Rare:253 | ||||
| chr12:27523989-27524249 | Rare:62 | ||||
| chr12:27710667-27710950 | Common:3; Rare:117 | ||||
| chr12:28190330-28190506 | Common:2; Rare:63 |