| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:2004319-2004669 | Common:2; Rare:125 | ||||
| chr12:2796696-2796767 | Common:1; Rare:11 | ||||
| chr12:2812509-2812714 | Common:1; Rare:50 | ||||
| chr12:2812885-2812984 | Rare:34 | ||||
| chr12:2835005-2835043 | Rare:12 | ||||
| chr12:2877031-2877271 | Rare:76 | ||||
| chr12:3077257-3077438 | Common:7; Rare:79 | ||||
| chr12:3873303-3873581 | Common:5; Rare:62 | ||||
| chr12:4273583-4274235 | Common:2; Rare:179; Clinvar (benign):1 | ||||
| chr12:4275433-4275709 | Common:3; Rare:50 | ||||
| chr12:4320947-4321266 | Common:5; Rare:122 | ||||
| chr12:4538431-4538939 | Common:3; Rare:116 | ||||
| chr12:4649010-4649158 | Common:2; Rare:53; Clinvar (benign):2 | ||||
| chr12:6124534-6124762 | Rare:30; Clinvar:1 | ||||
| chr12:6200031-6200545 | Common:4; Rare:151 |