| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:121399904-121400171 | Common:5; Rare:101 | ||||
| chr12:121712659-121712840 | Common:2; Rare:69 | ||||
| chr12:121793636-121793985 | Common:1; Rare:96 | ||||
| chr12:121802940-121803086 | Rare:35 | ||||
| chr12:122078969-122079190 | Common:1; Rare:43 | ||||
| chr12:122500817-122501122 | Common:2; Rare:84 | ||||
| chr12:122526849-122527281 | Common:4; Rare:156 | ||||
| chr12:122752450-122752949 | Common:1; Rare:161 | ||||
| chr12:122980590-122980743 | Common:1; Rare:51 | ||||
| chr12:123105457-123105669 | Common:1; Rare:39 | ||||
| chr12:123233093-123233486 | Common:2; Rare:128; Clinvar:1 | ||||
| chr12:123364797-123364977 | Common:4; Rare:74 | ||||
| chr12:123584454-123584657 | Common:1; Rare:93 | ||||
| chr12:123633624-123633851 | Common:1; Rare:104; Clinvar:8; Clinvar (benign):1 | ||||
| chr12:123972550-123972899 | Common:6; Rare:119 |