| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:122980226-122980281 | Rare:20 | ||||
| chr12:122980571-122980791 | Common:1; Rare:75 | ||||
| chr12:123233113-123233501 | Common:2; Rare:128; Clinvar:1 | ||||
| chr12:123364785-123364966 | Common:4; Rare:78 | ||||
| chr12:123436437-123436556 | Rare:18 | ||||
| chr12:123584278-123584748 | Common:8; Rare:157 | ||||
| chr12:123602062-123602139 | Common:3; Rare:25 | ||||
| chr12:123633624-123633860 | Common:1; Rare:110; Clinvar:8; Clinvar (benign):1 | ||||
| chr12:123972565-123972656 | Common:3; Rare:28 | ||||
| chr12:124786454-124786786 | Common:3; Rare:88 | ||||
| chr12:124914092-124914193 | Common:4; Rare:43 | ||||
| chr12:128823849-128824113 | Common:2; Rare:93 | ||||
| chr12:130871755-130872126 | Common:4; Rare:148 | ||||
| chr12:131710770-131711119 | Rare:98 | ||||
| chr12:131929050-131929291 | Common:10; Rare:73; Clinvar:1 |