| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:123533668-123533729 | Common:1; Rare:15 | ||||
| chr12:123584284-123584702 | Common:8; Rare:146 | ||||
| chr12:123584710-123584813 | Common:1; Rare:29 | ||||
| chr12:123602035-123602255 | Common:3; Rare:76 | ||||
| chr12:123618490-123618833 | Common:1; Rare:99 | ||||
| chr12:123633545-123633891 | Common:2; Rare:166; Clinvar:8; Clinvar (benign):1 | ||||
| chr12:123972529-123972639 | Common:2; Rare:29 | ||||
| chr12:123972674-123973352 | Common:5; Rare:218 | ||||
| chr12:124335252-124335516 | Common:4; Rare:72 | ||||
| chr12:124518183-124518351 | Common:2; Rare:39 | ||||
| chr12:124863774-124864075 | Common:1; Rare:82 | ||||
| chr12:124913721-124913973 | Common:3; Rare:103 | ||||
| chr12:124914056-124914251 | Common:7; Rare:77 | ||||
| chr12:124914777-124915048 | Common:3; Rare:108 | ||||
| chr12:124988917-124989181 | Common:2; Rare:81 |