| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:41921105-41921229 | Rare:32 | ||||
| chr6:42879605-42879934 | Rare:96 | ||||
| chr6:42929226-42929549 | Common:3; Rare:88 | ||||
| chr6:42984284-42984600 | Rare:76 | ||||
| chr6:43013869-43014297 | Common:2; Rare:96 | ||||
| chr6:43053787-43054052 | Common:1; Rare:74; Clinvar:5 | ||||
| chr6:43516861-43517109 | Common:4; Rare:94; Clinvar:2; Clinvar (benign):1 | ||||
| chr6:43575947-43576175 | Rare:89; Clinvar:4 | ||||
| chr6:43687757-43687912 | Common:2; Rare:59 | ||||
| chr6:43770081-43770254 | Common:3; Rare:52 | ||||
| chr6:43772606-43772933 | Common:1; Rare:47 | ||||
| chr6:44127351-44127663 | Common:4; Rare:91 | ||||
| chr6:44219466-44219651 | Common:1; Rare:50 | ||||
| chr6:44223478-44223618 | Common:1; Rare:45 | ||||
| chr6:44246882-44247187 | Common:4; Rare:126 |