| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:38905588-38905757 | Common:4; Rare:45 | ||||
| chr12:38906697-38907017 | Common:2; Rare:68 | ||||
| chr12:39443574-39443639 | Rare:9 | ||||
| chr12:40105462-40105694 | Common:2; Rare:74 | ||||
| chr12:40224535-40224759 | Common:1; Rare:61 | ||||
| chr12:40224812-40225010 | Common:5; Rare:49; Clinvar (benign):1 | ||||
| chr12:40225043-40225178 | Rare:50; Clinvar:1 | ||||
| chr12:42144531-42145012 | Common:10; Rare:195 | ||||
| chr12:42237484-42237741 | Rare:74 | ||||
| chr12:42237851-42237957 | Common:1; Rare:17 | ||||
| chr12:42238184-42238533 | Common:3; Rare:115 | ||||
| chr12:42238755-42238784 | Common:1; Rare:6 | ||||
| chr12:42325975-42326243 | Common:2; Rare:87 | ||||
| chr12:42589713-42589849 | Rare:52 | ||||
| chr12:42590045-42590113 | Rare:10 |