| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:50763925-50764298 | Common:1; Rare:98 | ||||
| chr12:51026313-51026510 | Common:3; Rare:89; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:51048103-51048366 | Common:2; Rare:92 | ||||
| chr12:51048415-51048447 | Rare:7 | ||||
| chr12:51198063-51198112 | Rare:3 | ||||
| chr12:51238574-51238918 | Common:8; Rare:129 | ||||
| chr12:51270165-51270327 | Common:2; Rare:41 | ||||
| chr12:52006754-52006946 | Rare:36 | ||||
| chr12:52051152-52051563 | Common:1; Rare:131 | ||||
| chr12:52070199-52070239 | Rare:13 | ||||
| chr12:52185102-52185571 | Common:2; Rare:132 | ||||
| chr12:52191601-52191746 | Rare:44 | ||||
| chr12:52301652-52301868 | Common:3; Rare:52 | ||||
| chr12:52367014-52367085 | Rare:19 | ||||
| chr12:52367139-52367229 | Common:1; Rare:33; Clinvar:1 |