| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:112013123-112013468 | Common:1; Rare:122 | ||||
| chr12:113185456-113185563 | Common:5; Rare:43 | ||||
| chr12:118136003-118136175 | Common:2; Rare:45 | ||||
| chr12:120194693-120194791 | Rare:37 | ||||
| chr12:120201081-120201366 | Common:2; Rare:90 | ||||
| chr12:120446359-120446478 | Common:1; Rare:53 | ||||
| chr12:120469568-120469867 | Common:2; Rare:107 | ||||
| chr12:120495852-120496139 | Common:4; Rare:92 | ||||
| chr12:120581358-120581586 | Common:1; Rare:79 | ||||
| chr12:121210087-121210152 | Rare:25 | ||||
| chr12:122526911-122527281 | Common:3; Rare:119 | ||||
| chr12:123233096-123233478 | Common:2; Rare:123; Clinvar:1 | ||||
| chr12:123364820-123364966 | Common:2; Rare:58 | ||||
| chr12:123584330-123584609 | Common:5; Rare:92 | ||||
| chr12:123633635-123633851 | Common:1; Rare:98; Clinvar:8; Clinvar (benign):1 |