| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6688949-6689137 | Rare:61 | ||||
| chr12:6689445-6689732 | Common:2; Rare:71 | ||||
| chr12:6723968-6724168 | Rare:51 | ||||
| chr12:6752937-6753164 | Common:5; Rare:64 | ||||
| chr12:6766409-6766748 | Rare:93 | ||||
| chr12:6869132-6869380 | Rare:81; Clinvar (benign):1; Clinvar (pathogenic):3 | ||||
| chr12:6873282-6873541 | Common:2; Rare:74 | ||||
| chr12:6943920-6944154 | Common:10; Rare:236; Clinvar:4; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr12:6967602-6967622 | Rare:6 | ||||
| chr12:6970621-6970957 | Common:3; Rare:105 | ||||
| chr12:7108367-7108600 | Common:2; Rare:79 | ||||
| chr12:7109132-7109224 | Rare:33 | ||||
| chr12:7130213-7130415 | Common:5; Rare:50 | ||||
| chr12:8032591-8032762 | Rare:62 | ||||
| chr12:8227563-8227709 | Rare:39 |