| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:37433190-37433275 | Common:1; Rare:24 | ||||
| chr6:39431328-39431412 | Common:1; Rare:19 | ||||
| chr6:41072616-41072981 | Rare:98 | ||||
| chr6:41921108-41921276 | Rare:44 | ||||
| chr6:42928888-42929190 | Rare:73 | ||||
| chr6:42929209-42929561 | Common:4; Rare:99 | ||||
| chr6:43013883-43014294 | Common:2; Rare:90 | ||||
| chr6:43059820-43059890 | Rare:23 | ||||
| chr6:43516775-43517109 | Common:6; Rare:120; Clinvar:2; Clinvar (benign):1 | ||||
| chr6:43575983-43576141 | Rare:52 | ||||
| chr6:44127358-44127639 | Common:4; Rare:78 | ||||
| chr6:44387655-44387725 | Common:2; Rare:23 | ||||
| chr6:46652708-46652989 | Rare:74 | ||||
| chr6:49463192-49463376 | Common:1; Rare:54; Clinvar:1; Clinvar (benign):1 | ||||
| chr6:52576935-52577307 | Common:7; Rare:132 |