| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:31324134-31324265 | Rare:31 | ||||
| chr12:31325372-31325684 | Rare:56 | ||||
| chr12:31326036-31326477 | Common:4; Rare:139 | ||||
| chr12:31659139-31659258 | Common:1; Rare:37 | ||||
| chr12:31728995-31729319 | Common:1; Rare:102 | ||||
| chr12:31959248-31959621 | Common:3; Rare:123 | ||||
| chr12:32399002-32399692 | Common:9; Rare:164 | ||||
| chr12:32399707-32399958 | Common:1; Rare:77 | ||||
| chr12:32400344-32400388 | Common:1; Rare:12 | ||||
| chr12:32730819-32731069 | Common:2; Rare:30; Clinvar:1; Clinvar (benign):2 | ||||
| chr12:32755186-32755318 | Common:1; Rare:34; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr12:32755826-32756013 | Rare:71 | ||||
| chr12:32756344-32756499 | Rare:33 | ||||
| chr12:32896754-32897057 | Common:3; Rare:99; Clinvar:4; Clinvar (benign):3 | ||||
| chr12:33439807-33440102 | Common:2; Rare:97 |