| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:20369686-20369717 | Rare:6 | ||||
| chr12:21437531-21438084 | Common:8; Rare:200 | ||||
| chr12:21438168-21438315 | Common:1; Rare:31 | ||||
| chr12:21501263-21501395 | Common:1; Rare:36 | ||||
| chr12:21501517-21501924 | Common:6; Rare:117 | ||||
| chr12:21502008-21502109 | Common:2; Rare:22 | ||||
| chr12:21502224-21502399 | Common:1; Rare:36 | ||||
| chr12:21656981-21657097 | Common:1; Rare:23 | ||||
| chr12:21657641-21658045 | Common:5; Rare:120; Clinvar:2; Clinvar (benign):1 | ||||
| chr12:22046145-22046319 | Rare:60 | ||||
| chr12:22046548-22046610 | Rare:22 | ||||
| chr12:22046760-22046795 | Rare:9 | ||||
| chr12:22544142-22544383 | Common:1; Rare:110 | ||||
| chr12:22544412-22544747 | Common:2; Rare:79 | ||||
| chr12:22624968-22625299 | Common:1; Rare:148 |