| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:31073732-31073902 | Common:8; Rare:61 | ||||
| chr12:31074079-31074276 | Common:1; Rare:40 | ||||
| chr12:31324062-31324423 | Rare:85 | ||||
| chr12:31326083-31326423 | Common:3; Rare:99 | ||||
| chr12:31728993-31729365 | Common:1; Rare:117 | ||||
| chr12:31958965-31959179 | Common:1; Rare:49 | ||||
| chr12:31959258-31959490 | Common:2; Rare:75 | ||||
| chr12:32399187-32399611 | Common:5; Rare:114 | ||||
| chr12:32399750-32400197 | Common:4; Rare:124 | ||||
| chr12:32502406-32502537 | Rare:15 | ||||
| chr12:32679109-32679465 | Common:1; Rare:129; Clinvar:1; Clinvar (benign):4 | ||||
| chr12:32733491-32733807 | Common:1; Rare:51; Clinvar:1; Clinvar (benign):1 | ||||
| chr12:32739972-32740088 | Rare:40; Clinvar (benign):2 | ||||
| chr12:32755870-32755985 | Rare:45 | ||||
| chr12:32896760-32896990 | Common:2; Rare:78; Clinvar:4; Clinvar (benign):3 |