| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:57746021-57746253 | Rare:68 | ||||
| chr12:57772079-57772240 | Rare:59 | ||||
| chr12:57772516-57772670 | Common:3; Rare:23 | ||||
| chr12:57772852-57772967 | Rare:30 | ||||
| chr12:57846702-57846988 | Common:2; Rare:98 | ||||
| chr12:57941360-57941693 | Common:3; Rare:97 | ||||
| chr12:58920491-58920704 | Common:2; Rare:72 | ||||
| chr12:59595815-59596180 | Common:7; Rare:80 | ||||
| chr12:62260165-62260427 | Common:1; Rare:94 | ||||
| chr12:64222242-64222392 | Rare:50 | ||||
| chr12:64404226-64404588 | Common:4; Rare:140 | ||||
| chr12:64452025-64452174 | Common:1; Rare:55 | ||||
| chr12:64759151-64759531 | Common:1; Rare:122; Clinvar:6; Clinvar (benign):2 | ||||
| chr12:65169441-65169588 | Common:1; Rare:47 | ||||
| chr12:65824072-65824444 | Common:2; Rare:90 |