| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:16347484-16347685 | Common:4; Rare:36 | ||||
| chr12:16347697-16347727 | Rare:6 | ||||
| chr12:19439339-19439743 | Common:3; Rare:149 | ||||
| chr12:19440428-19440683 | Common:2; Rare:87 | ||||
| chr12:21437531-21437804 | Common:7; Rare:105 | ||||
| chr12:21438263-21438348 | Common:1; Rare:20 | ||||
| chr12:21501253-21501431 | Common:1; Rare:43 | ||||
| chr12:21501565-21501889 | Common:1; Rare:81 | ||||
| chr12:21502317-21502355 | Rare:7 | ||||
| chr12:21527793-21527936 | Common:1; Rare:45 | ||||
| chr12:21528063-21528123 | Rare:15 | ||||
| chr12:21656688-21657105 | Common:6; Rare:74 | ||||
| chr12:21657739-21658087 | Common:4; Rare:104; Clinvar:2; Clinvar (benign):1 | ||||
| chr12:21941317-21941362 | Rare:15 | ||||
| chr12:22046187-22046360 | Rare:50 |