| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:28190360-28190524 | Common:1; Rare:53 | ||||
| chr12:29149019-29149323 | Rare:88 | ||||
| chr12:29381143-29381387 | Common:3; Rare:74 | ||||
| chr12:30754749-30755041 | Common:1; Rare:116 | ||||
| chr12:31073716-31073896 | Common:7; Rare:65 | ||||
| chr12:31728990-31729288 | Common:1; Rare:92 | ||||
| chr12:31959262-31959482 | Common:2; Rare:70 | ||||
| chr12:32534245-32534403 | Common:2; Rare:32 | ||||
| chr12:32679063-32679366 | Common:2; Rare:122; Clinvar:1; Clinvar (benign):4 | ||||
| chr12:32755878-32756047 | Common:1; Rare:54 | ||||
| chr12:32896760-32896990 | Common:2; Rare:78; Clinvar:4; Clinvar (benign):3 | ||||
| chr12:38905506-38905730 | Common:3; Rare:61 | ||||
| chr12:38906276-38906405 | Common:1; Rare:31 | ||||
| chr12:38906763-38906876 | Rare:23 | ||||
| chr12:39442966-39443222 | Common:2; Rare:65; Clinvar:5; Clinvar (benign):5 |