| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:19439873-19440073 | Common:1; Rare:91 | ||||
| chr12:20369548-20369708 | Common:2; Rare:67 | ||||
| chr12:20369715-20369908 | Common:1; Rare:94 | ||||
| chr12:21501509-21501948 | Common:6; Rare:125 | ||||
| chr12:21657745-21657899 | Common:2; Rare:61; Clinvar:2; Clinvar (benign):1 | ||||
| chr12:22046472-22046552 | Rare:24 | ||||
| chr12:22544158-22544326 | Common:1; Rare:87 | ||||
| chr12:22544474-22544677 | Common:2; Rare:46 | ||||
| chr12:22624972-22625208 | Common:1; Rare:106 | ||||
| chr12:24948983-24949162 | Common:1; Rare:43 | ||||
| chr12:25195084-25195340 | Common:2; Rare:79 | ||||
| chr12:25251007-25251299 | Rare:74 | ||||
| chr12:26937909-26938706 | Common:12; Rare:256 | ||||
| chr12:27332721-27332962 | Common:2; Rare:75 | ||||
| chr12:27524003-27524349 | Rare:80 |