| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:21657758-21658050 | Common:4; Rare:93; Clinvar:2; Clinvar (benign):1 | ||||
| chr12:22046116-22046307 | Common:2; Rare:69 | ||||
| chr12:22544171-22544365 | Common:1; Rare:89 | ||||
| chr12:22544544-22544736 | Common:1; Rare:39 | ||||
| chr12:22624996-22625254 | Common:1; Rare:123 | ||||
| chr12:25195094-25195409 | Common:2; Rare:94 | ||||
| chr12:25250903-25251335 | Rare:116; Clinvar:3; Clinvar (benign):1 | ||||
| chr12:25648234-25648495 | Rare:49 | ||||
| chr12:25648540-25648900 | Common:3; Rare:77 | ||||
| chr12:25958435-25958720 | Common:1; Rare:110 | ||||
| chr12:26125030-26125265 | Common:1; Rare:56 | ||||
| chr12:26833027-26833506 | Common:3; Rare:128 | ||||
| chr12:26937897-26938166 | Common:7; Rare:74 | ||||
| chr12:26938272-26938542 | Common:3; Rare:102 | ||||
| chr12:27014280-27014521 | Common:1; Rare:71 |