| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:31324068-31324780 | Common:3; Rare:266 | ||||
| chr12:31325262-31325440 | Rare:57 | ||||
| chr12:31325521-31325699 | Rare:56 | ||||
| chr12:31326019-31326530 | Common:8; Rare:286 | ||||
| chr12:31589620-31590050 | Common:2; Rare:166 | ||||
| chr12:31590670-31591450 | Common:5; Rare:502 | ||||
| chr12:31658960-31659724 | Common:8; Rare:389 | ||||
| chr12:31715080-31715590 | Common:6; Rare:87 | ||||
| chr12:31728706-31729404 | Common:6; Rare:432 | ||||
| chr12:31959249-31959608 | Common:7; Rare:249 | ||||
| chr12:32106604-32107001 | Common:16; Rare:275 | ||||
| chr12:32399231-32399703 | Common:10; Rare:194 | ||||
| chr12:32399719-32400071 | Common:4; Rare:211 | ||||
| chr12:32679022-32679363 | Common:6; Rare:346; Clinvar:1; Clinvar (benign):10 | ||||
| chr12:32679480-32679906 | Common:4; Rare:192 |