| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:32399793-32399970 | Common:1; Rare:55 | ||||
| chr12:32896599-32896996 | Common:5; Rare:126; Clinvar:7; Clinvar (benign):9 | ||||
| chr12:38905491-38905702 | Common:3; Rare:60 | ||||
| chr12:38906754-38906847 | Common:1; Rare:21 | ||||
| chr12:39619783-39620096 | Common:1; Rare:52 | ||||
| chr12:40224667-40225076 | Common:5; Rare:96; Clinvar (benign):1 | ||||
| chr12:42325934-42326215 | Common:1; Rare:88 | ||||
| chr12:43758749-43759021 | Common:2; Rare:76; Clinvar:2 | ||||
| chr12:43806210-43806397 | Common:2; Rare:60 | ||||
| chr12:45215998-45216204 | Rare:64 | ||||
| chr12:45729535-45729747 | Rare:63 | ||||
| chr12:45990374-45990917 | Common:2; Rare:173 | ||||
| chr12:45991951-45992128 | Common:2; Rare:49 | ||||
| chr12:46268397-46269205 | Common:3; Rare:199 | ||||
| chr12:46362296-46362523 | Common:2; Rare:60 |