| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:21275-21409 | Common:2; Rare:8 | ||||
| chr12:537816-538082 | Rare:46 | ||||
| chr12:539188-539427 | Common:1; Rare:37 | ||||
| chr12:590296-590463 | Rare:30 | ||||
| chr12:753820-754088 | Common:2; Rare:105; Clinvar:7; Clinvar (benign):4 | ||||
| chr12:754265-754294 | Rare:5 | ||||
| chr12:754319-754386 | Common:4; Rare:13; Clinvar (benign):2 | ||||
| chr12:763811-763912 | Rare:21 | ||||
| chr12:778661-778806 | Common:1; Rare:31 | ||||
| chr12:838801-839023 | Common:2; Rare:34 | ||||
| chr12:864721-865057 | Common:3; Rare:61 | ||||
| chr12:865465-865798 | Common:2; Rare:61 | ||||
| chr12:897421-897530 | Common:1; Rare:28; Clinvar:1 | ||||
| chr12:911433-911518 | Common:1; Rare:10 | ||||
| chr12:917585-917748 | Common:1; Rare:20 |