| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:107903637-107903974 | Common:7; Rare:114 | ||||
| chr12:108313891-108313991 | Common:2; Rare:15 | ||||
| chr12:108334315-108334404 | Rare:15 | ||||
| chr12:108335717-108336067 | Common:2; Rare:52 | ||||
| chr12:108511793-108511915 | Common:1; Rare:19 | ||||
| chr12:108541308-108541605 | Common:1; Rare:62 | ||||
| chr12:108563535-108563828 | Common:2; Rare:58 | ||||
| chr12:108566037-108566278 | Common:1; Rare:48 | ||||
| chr12:108566306-108566315 | Rare:1 | ||||
| chr12:108568869-108568957 | Rare:22; Clinvar:1; Clinvar (benign):2 | ||||
| chr12:108569850-108570188 | Common:1; Rare:67 | ||||
| chr12:108571885-108572070 | Common:1; Rare:32 | ||||
| chr12:108572405-108572648 | Common:1; Rare:46 | ||||
| chr12:108573321-108573581 | Common:1; Rare:42 | ||||
| chr12:108609541-108609562 | Rare:4 |