| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:2794874-2795145 | Common:1; Rare:96 | ||||
| chr12:2812489-2812713 | Common:1; Rare:52 | ||||
| chr12:2877023-2877253 | Rare:67 | ||||
| chr12:4320979-4321236 | Common:4; Rare:92 | ||||
| chr12:4538455-4538798 | Rare:70 | ||||
| chr12:4649039-4649154 | Common:1; Rare:47; Clinvar (benign):1 | ||||
| chr12:6493244-6493381 | Common:5; Rare:38 | ||||
| chr12:6493796-6494126 | Common:2; Rare:100 | ||||
| chr12:6534270-6534582 | Common:5; Rare:131 | ||||
| chr12:6534651-6534841 | Common:3; Rare:76 | ||||
| chr12:6663107-6663403 | Common:2; Rare:79 | ||||
| chr12:6724011-6724135 | Rare:34 | ||||
| chr12:6753066-6753189 | Common:4; Rare:47 | ||||
| chr12:6851890-6852174 | Rare:72 | ||||
| chr12:6867403-6867550 | Common:2; Rare:63; Clinvar:1; Clinvar (benign):2 |