| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6051853-6051950 | Rare:15 | ||||
| chr12:6068963-6069071 | Rare:16 | ||||
| chr12:6071575-6071826 | Common:1; Rare:43 | ||||
| chr12:6072321-6072641 | Common:1; Rare:79; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:6074427-6074543 | Common:1; Rare:20 | ||||
| chr12:6075008-6075287 | Rare:70 | ||||
| chr12:6094941-6095628 | Common:6; Rare:151; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:6104394-6104495 | Common:1; Rare:20 | ||||
| chr12:6116630-6116892 | Common:4; Rare:53 | ||||
| chr12:6119873-6119895 | Rare:5 | ||||
| chr12:6121372-6121394 | Common:2; Rare:3 | ||||
| chr12:6121480-6121541 | Rare:8 | ||||
| chr12:6122545-6122675 | Rare:22 | ||||
| chr12:6122984-6123611 | Common:2; Rare:162; Clinvar:2; Clinvar (benign):1 | ||||
| chr12:6123630-6123857 | Common:1; Rare:47 |