| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:49188486-49188636 | Common:2; Rare:21 | ||||
| chr12:49188981-49189274 | Rare:81; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:49322984-49323337 | Common:3; Rare:79 | ||||
| chr12:49367179-49367571 | Common:1; Rare:108 | ||||
| chr12:49568069-49568192 | Common:2; Rare:43 | ||||
| chr12:49741378-49741587 | Rare:61 | ||||
| chr12:49828398-49828571 | Rare:60 | ||||
| chr12:49843090-49843130 | Rare:13 | ||||
| chr12:50025402-50025747 | Common:2; Rare:92 | ||||
| chr12:50085149-50085384 | Common:1; Rare:67 | ||||
| chr12:50167284-50167648 | Common:3; Rare:105 | ||||
| chr12:50283515-50283672 | Common:3; Rare:47 | ||||
| chr12:50400747-50401016 | Common:1; Rare:91 | ||||
| chr12:50763925-50764128 | Common:1; Rare:57 | ||||
| chr12:51026313-51026517 | Common:3; Rare:91; Clinvar:2; Clinvar (benign):2 |