| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:31074056-31074271 | Common:1; Rare:47 | ||||
| chr12:31324137-31324316 | Rare:36 | ||||
| chr12:31326041-31326456 | Common:4; Rare:135 | ||||
| chr12:31729012-31729292 | Common:1; Rare:84 | ||||
| chr12:31959276-31959488 | Common:2; Rare:68 | ||||
| chr12:32399706-32399956 | Common:1; Rare:77 | ||||
| chr12:32755853-32755997 | Rare:56 | ||||
| chr12:32896727-32897074 | Common:4; Rare:109; Clinvar:4; Clinvar (benign):6 | ||||
| chr12:38905580-38905712 | Common:3; Rare:37 | ||||
| chr12:39443310-39443499 | Rare:63; Clinvar:2; Clinvar (benign):1 | ||||
| chr12:42326015-42326215 | Common:1; Rare:65 | ||||
| chr12:42483916-42484093 | Common:1; Rare:24 | ||||
| chr12:43758740-43758995 | Common:2; Rare:71; Clinvar:2 | ||||
| chr12:43806249-43806385 | Common:2; Rare:47 | ||||
| chr12:44876189-44876459 | Common:2; Rare:91 |