| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:130314395-130314528 | Common:1; Rare:46 | ||||
| chr11:130916411-130916629 | Common:6; Rare:72 | ||||
| chr11:134224547-134224698 | Rare:58 | ||||
| chr11:134225425-134225644 | Rare:65 | ||||
| chr11:134253290-134253606 | Common:2; Rare:116; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr11:134276169-134276268 | Common:1; Rare:17 | ||||
| chr11:134287075-134287103 | Common:1; Rare:14 | ||||
| chr12:389236-389383 | Rare:57 | ||||
| chr12:389521-389610 | Common:5; Rare:40 | ||||
| chr12:401434-401655 | Common:1; Rare:60 | ||||
| chr12:643624-643708 | Rare:15 | ||||
| chr12:752323-752597 | Common:1; Rare:77 | ||||
| chr12:991101-991322 | Common:3; Rare:100 | ||||
| chr12:1593027-1593062 | Rare:10 | ||||
| chr12:1690861-1691048 | Common:1; Rare:60 |