| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:120446368-120446478 | Common:1; Rare:50 | ||||
| chr12:120469555-120469867 | Common:2; Rare:111 | ||||
| chr12:120495907-120496169 | Common:5; Rare:82 | ||||
| chr12:121399904-121400144 | Common:5; Rare:88 | ||||
| chr12:121802943-121803091 | Rare:34 | ||||
| chr12:122526849-122527281 | Common:4; Rare:156 | ||||
| chr12:122980571-122980723 | Rare:49 | ||||
| chr12:123233093-123233478 | Common:2; Rare:125; Clinvar:1 | ||||
| chr12:123364820-123364928 | Common:1; Rare:44 | ||||
| chr12:123584290-123584595 | Common:6; Rare:96 | ||||
| chr12:123601829-123602156 | Common:6; Rare:89 | ||||
| chr12:123633632-123633851 | Common:1; Rare:100; Clinvar:8; Clinvar (benign):1 | ||||
| chr12:123973017-123973328 | Common:2; Rare:102 | ||||
| chr12:132887566-132887798 | Rare:65 | ||||
| chr12:132956304-132956435 | Rare:24 |