| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:124423016-124423332 | Common:2; Rare:78 | ||||
| chr12:124914047-124914193 | Common:6; Rare:63 | ||||
| chr12:132687309-132687704 | Common:4; Rare:148; Clinvar:6; Clinvar (benign):10; Clinvar (pathogenic):1 | ||||
| chr12:132710594-132710850 | Common:4; Rare:96 | ||||
| chr12:132887558-132887794 | Rare:71 | ||||
| chr12:132956260-132956422 | Common:1; Rare:34 | ||||
| chr12:133130403-133130621 | Common:4; Rare:71 | ||||
| chr13:19863491-19863840 | Common:5; Rare:126 | ||||
| chr13:21176545-21176738 | Common:1; Rare:98 | ||||
| chr13:23579234-23579471 | Common:4; Rare:73 | ||||
| chr13:23889289-23889465 | Rare:61 | ||||
| chr13:25301452-25301689 | Common:1; Rare:93 | ||||
| chr13:26221798-26221970 | Rare:50 | ||||
| chr13:27251245-27251623 | Common:6; Rare:114 | ||||
| chr13:27450130-27450212 | Common:2; Rare:23 |