| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:114408000-114408198 | Common:1; Rare:36; Clinvar (benign):2 | ||||
| chr12:114408644-114408757 | Rare:24 | ||||
| chr12:114683963-114684304 | Common:3; Rare:98; Clinvar:2 | ||||
| chr12:114684497-114684622 | Rare:35 | ||||
| chr12:118016536-118016789 | Common:2; Rare:50 | ||||
| chr12:118135953-118136190 | Common:2; Rare:73 | ||||
| chr12:120201085-120201354 | Common:2; Rare:86 | ||||
| chr12:120437863-120438164 | Common:2; Rare:107; Clinvar (benign):2 | ||||
| chr12:120446357-120446470 | Common:1; Rare:49 | ||||
| chr12:120469555-120469895 | Common:3; Rare:119 | ||||
| chr12:120495859-120496228 | Common:7; Rare:125 | ||||
| chr12:120581358-120581577 | Common:1; Rare:77 | ||||
| chr12:121210067-121210152 | Common:1; Rare:30 | ||||
| chr12:121399885-121400144 | Common:5; Rare:93 | ||||
| chr12:121672601-121672702 | Common:4; Rare:33 |