| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:43053763-43053995 | Common:2; Rare:78; Clinvar:5; Clinvar (benign):1 | ||||
| chr6:43059820-43059926 | Common:1; Rare:36 | ||||
| chr6:43060186-43060594 | Common:2; Rare:99 | ||||
| chr6:43427469-43427599 | Rare:39 | ||||
| chr6:43516854-43517112 | Common:5; Rare:96; Clinvar:2; Clinvar (benign):1 | ||||
| chr6:43575962-43576275 | Common:1; Rare:123; Clinvar:9 | ||||
| chr6:43625490-43625803 | Rare:77 | ||||
| chr6:43629137-43629495 | Common:2; Rare:101 | ||||
| chr6:43687757-43687850 | Common:1; Rare:40 | ||||
| chr6:43770087-43770415 | Common:5; Rare:87 | ||||
| chr6:43771670-43771996 | Common:4; Rare:59 | ||||
| chr6:43773436-43773572 | Common:2; Rare:23 | ||||
| chr6:44126579-44126699 | Common:1; Rare:27 | ||||
| chr6:44127351-44127669 | Common:4; Rare:92 | ||||
| chr6:44219496-44219674 | Common:2; Rare:47 |