| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:120469472-120469924 | Common:5; Rare:152 | ||||
| chr12:120495828-120496151 | Common:7; Rare:102 | ||||
| chr12:120528871-120529016 | Rare:54 | ||||
| chr12:120529086-120529282 | Common:2; Rare:71 | ||||
| chr12:120529394-120529482 | Rare:17 | ||||
| chr12:120534202-120534404 | Common:1; Rare:62 | ||||
| chr12:120534916-120535057 | Common:1; Rare:55 | ||||
| chr12:120581279-120581590 | Common:1; Rare:118 | ||||
| chr12:120640435-120640758 | Rare:77 | ||||
| chr12:120686320-120686624 | Common:3; Rare:85 | ||||
| chr12:120686773-120687224 | Common:2; Rare:139 | ||||
| chr12:120696757-120696886 | Common:1; Rare:16 | ||||
| chr12:120710341-120710541 | Common:3; Rare:75 | ||||
| chr12:120710663-120710996 | Common:1; Rare:79 | ||||
| chr12:120725650-120725934 | Common:3; Rare:89; Clinvar:1; Clinvar (pathogenic):2 |