| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:21437615-21437806 | Common:4; Rare:86 | ||||
| chr12:21437850-21438019 | Common:1; Rare:109 | ||||
| chr12:21501526-21501833 | Common:4; Rare:82 | ||||
| chr12:21502028-21502128 | Common:3; Rare:15 | ||||
| chr12:21657171-21657571 | Common:1; Rare:110 | ||||
| chr12:21657786-21657997 | Common:4; Rare:73; Clinvar:2; Clinvar (benign):1 | ||||
| chr12:21774425-21774569 | Rare:41; Clinvar (benign):1 | ||||
| chr12:21774781-21775105 | Rare:64 | ||||
| chr12:21910655-21911055 | Common:5; Rare:110; Clinvar:10; Clinvar (benign):5 | ||||
| chr12:22046114-22046304 | Common:2; Rare:70 | ||||
| chr12:22334189-22334769 | Common:6; Rare:164 | ||||
| chr12:22334825-22335039 | Rare:70 | ||||
| chr12:22335100-22335530 | Common:4; Rare:101 | ||||
| chr12:22335645-22335776 | Rare:30 | ||||
| chr12:22544187-22544304 | Common:1; Rare:55 |