| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:3753107-3753245 | Rare:36 | ||||
| chr12:3873303-3873527 | Common:4; Rare:48 | ||||
| chr12:4320949-4321258 | Common:5; Rare:117 | ||||
| chr12:4538431-4538907 | Common:1; Rare:106 | ||||
| chr12:4649049-4649154 | Common:1; Rare:45; Clinvar (benign):1 | ||||
| chr12:6124407-6124762 | Rare:53; Clinvar:2 | ||||
| chr12:6200005-6200480 | Common:4; Rare:138 | ||||
| chr12:6383980-6384284 | Common:2; Rare:69 | ||||
| chr12:6384824-6385135 | Common:2; Rare:70 | ||||
| chr12:6452080-6452125 | Common:1; Rare:13 | ||||
| chr12:6470655-6470839 | Rare:50 | ||||
| chr12:6493107-6493381 | Common:7; Rare:86 | ||||
| chr12:6493763-6494126 | Common:2; Rare:107 | ||||
| chr12:6534256-6534578 | Common:6; Rare:129 | ||||
| chr12:6536526-6536788 | Rare:91 |