| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6723970-6724295 | Rare:80 | ||||
| chr12:6752932-6753191 | Common:6; Rare:79 | ||||
| chr12:6766310-6766748 | Rare:129 | ||||
| chr12:6851269-6851504 | Rare:50 | ||||
| chr12:6851879-6852174 | Rare:78 | ||||
| chr12:6867374-6867680 | Common:2; Rare:144; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:6868919-6869181 | Rare:78; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr12:6869418-6869744 | Common:1; Rare:93; Clinvar (pathogenic):1 | ||||
| chr12:6873282-6873546 | Common:2; Rare:76 | ||||
| chr12:6914430-6914597 | Rare:46 | ||||
| chr12:6943525-6943818 | Common:4; Rare:122 | ||||
| chr12:6959222-6959332 | Rare:24 | ||||
| chr12:6970219-6970494 | Common:1; Rare:97 | ||||
| chr12:6970510-6970988 | Common:4; Rare:153; Clinvar (benign):1 | ||||
| chr12:7018431-7018542 | Rare:37 |