| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:132675848-132676142 | Common:2; Rare:75; Clinvar:5; Clinvar (benign):6 | ||||
| chr12:132687303-132687696 | Common:4; Rare:145; Clinvar:7; Clinvar (benign):10; Clinvar (pathogenic):1 | ||||
| chr12:132710557-132710842 | Common:4; Rare:103 | ||||
| chr12:132829076-132829241 | Rare:77 | ||||
| chr12:132887553-132887859 | Rare:91 | ||||
| chr12:132956252-132956426 | Common:1; Rare:38 | ||||
| chr12:132986284-132986448 | Rare:39 | ||||
| chr12:133080237-133080459 | Common:5; Rare:66 | ||||
| chr12:133080732-133080954 | Rare:68 | ||||
| chr12:133130238-133130652 | Common:7; Rare:137 | ||||
| chr13:19633373-19633751 | Common:1; Rare:142 | ||||
| chr13:19659139-19659277 | Rare:35 | ||||
| chr13:19863441-19863653 | Common:3; Rare:69 | ||||
| chr13:19863655-19863813 | Common:2; Rare:52 | ||||
| chr13:19958468-19958846 | Common:6; Rare:174 |