| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:2812880-2813057 | Rare:50 | ||||
| chr12:2877015-2877253 | Rare:71 | ||||
| chr12:2890697-2890923 | Common:1; Rare:84 | ||||
| chr12:3753088-3753245 | Common:1; Rare:40 | ||||
| chr12:3873367-3873514 | Common:1; Rare:34 | ||||
| chr12:4320933-4321258 | Common:5; Rare:124 | ||||
| chr12:4538440-4538956 | Common:3; Rare:123 | ||||
| chr12:4649011-4649154 | Common:2; Rare:50; Clinvar (benign):1 | ||||
| chr12:6342065-6342117 | Rare:14 | ||||
| chr12:6444838-6445008 | Rare:30 | ||||
| chr12:6452043-6452150 | Common:1; Rare:25 | ||||
| chr12:6470623-6470839 | Common:1; Rare:74 | ||||
| chr12:6493186-6493502 | Common:8; Rare:92 | ||||
| chr12:6493544-6494146 | Common:4; Rare:151 | ||||
| chr12:6534308-6534582 | Common:5; Rare:118 |