| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:55966588-55966891 | Rare:80 | ||||
| chr12:55973954-55974192 | Common:2; Rare:66 | ||||
| chr12:55997046-55997381 | Common:2; Rare:87; Clinvar:2 | ||||
| chr12:56007262-56007517 | Common:1; Rare:52 | ||||
| chr12:56041558-56042235 | Common:6; Rare:187; Clinvar:3; Clinvar (benign):6 | ||||
| chr12:56042339-56042389 | Rare:20 | ||||
| chr12:56104146-56104664 | Common:4; Rare:166 | ||||
| chr12:56104956-56105227 | Common:1; Rare:57 | ||||
| chr12:56116019-56116086 | Rare:14 | ||||
| chr12:56116429-56116765 | Common:3; Rare:137 | ||||
| chr12:56117899-56118636 | Common:2; Rare:184 | ||||
| chr12:56127859-56128384 | Rare:117 | ||||
| chr12:56128579-56128684 | Rare:34 | ||||
| chr12:56151749-56151905 | Common:1; Rare:30 | ||||
| chr12:56151960-56152122 | Common:1; Rare:31 |