| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:24902289-24902335 | Rare:9 | ||||
| chr12:25195132-25195308 | Common:2; Rare:51 | ||||
| chr12:26937961-26938183 | Common:8; Rare:65 | ||||
| chr12:26938309-26938534 | Common:3; Rare:88 | ||||
| chr12:27244034-27244304 | Common:2; Rare:84 | ||||
| chr12:27523989-27524270 | Rare:66 | ||||
| chr12:27710748-27710853 | Common:1; Rare:43 | ||||
| chr12:28190389-28190524 | Common:1; Rare:42 | ||||
| chr12:30695870-30695964 | Common:1; Rare:24 | ||||
| chr12:31073743-31073907 | Common:8; Rare:61 | ||||
| chr12:31326163-31326456 | Common:4; Rare:99 | ||||
| chr12:31728995-31729175 | Rare:60 | ||||
| chr12:31959271-31959455 | Common:2; Rare:59 | ||||
| chr12:32679080-32679358 | Common:2; Rare:112; Clinvar:1; Clinvar (benign):4 | ||||
| chr12:32755884-32756028 | Common:1; Rare:45 |