| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:118135938-118136190 | Common:2; Rare:80 | ||||
| chr12:118190453-118190620 | Common:1; Rare:34 | ||||
| chr12:118372820-118373150 | Common:2; Rare:86 | ||||
| chr12:118981302-118981545 | Rare:75 | ||||
| chr12:119179337-119179634 | Rare:107; Clinvar:9; Clinvar (benign):3 | ||||
| chr12:119667745-119667987 | Common:2; Rare:67 | ||||
| chr12:119803341-119803562 | Rare:69; Clinvar (pathogenic):1 | ||||
| chr12:119877261-119877623 | Common:2; Rare:78 | ||||
| chr12:120194693-120194798 | Rare:39 | ||||
| chr12:120201085-120201372 | Common:2; Rare:89 | ||||
| chr12:120437826-120438350 | Common:3; Rare:176; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr12:120446353-120446474 | Common:1; Rare:55 | ||||
| chr12:120469624-120469895 | Common:3; Rare:95 | ||||
| chr12:120495845-120496228 | Common:7; Rare:128 | ||||
| chr12:120534276-120534363 | Common:1; Rare:30 |