| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:27710738-27710853 | Common:1; Rare:45 | ||||
| chr12:27780800-27780896 | Rare:26 | ||||
| chr12:28190367-28190506 | Common:1; Rare:44 | ||||
| chr12:28190718-28190829 | Common:1; Rare:35 | ||||
| chr12:29381121-29381375 | Common:3; Rare:81 | ||||
| chr12:30695819-30696014 | Common:2; Rare:50 | ||||
| chr12:30754762-30755033 | Common:1; Rare:106 | ||||
| chr12:31073784-31073892 | Rare:44 | ||||
| chr12:31324092-31324261 | Rare:41 | ||||
| chr12:31729010-31729308 | Common:1; Rare:93 | ||||
| chr12:31959284-31959488 | Common:2; Rare:65 | ||||
| chr12:32733467-32733804 | Common:1; Rare:57; Clinvar:1; Clinvar (benign):1 | ||||
| chr12:32755878-32756014 | Rare:45 | ||||
| chr12:38905560-38905742 | Common:3; Rare:46 | ||||
| chr12:38906287-38906372 | Common:1; Rare:23 |