| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:19439982-19440173 | Rare:69 | ||||
| chr12:19440461-19440693 | Common:2; Rare:82 | ||||
| chr12:19440706-19440801 | Rare:40 | ||||
| chr12:21437522-21438008 | Common:8; Rare:189 | ||||
| chr12:21438153-21438396 | Common:1; Rare:47 | ||||
| chr12:21501241-21501400 | Common:1; Rare:43 | ||||
| chr12:21501505-21501934 | Common:6; Rare:122 | ||||
| chr12:21502206-21502242 | Rare:12 | ||||
| chr12:21502284-21502369 | Rare:17 | ||||
| chr12:21526170-21526360 | Rare:27 | ||||
| chr12:21527781-21527972 | Common:1; Rare:64 | ||||
| chr12:21656966-21657128 | Common:1; Rare:36 | ||||
| chr12:21657753-21658027 | Common:4; Rare:90; Clinvar:2; Clinvar (benign):1 | ||||
| chr12:22046145-22046391 | Rare:73 | ||||
| chr12:22046707-22046885 | Rare:37 |