| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:38905526-38905732 | Common:3; Rare:57 | ||||
| chr12:38905733-38905777 | Common:1; Rare:14 | ||||
| chr12:39619761-39620093 | Common:1; Rare:53 | ||||
| chr12:40224860-40225060 | Common:4; Rare:50; Clinvar (benign):1 | ||||
| chr12:42238153-42238562 | Common:5; Rare:127 | ||||
| chr12:42326065-42326206 | Common:1; Rare:43 | ||||
| chr12:43758745-43758991 | Common:2; Rare:67; Clinvar:2 | ||||
| chr12:45216007-45216168 | Rare:51 | ||||
| chr12:45990504-45990959 | Common:2; Rare:148 | ||||
| chr12:46362296-46362635 | Common:2; Rare:91 | ||||
| chr12:46372594-46372942 | Rare:133 | ||||
| chr12:47079511-47079629 | Common:1; Rare:24 | ||||
| chr12:47705960-47706124 | Rare:70 | ||||
| chr12:47758166-47758316 | Common:1; Rare:21 | ||||
| chr12:47758708-47759077 | Common:2; Rare:68 |