| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:43629143-43629464 | Common:2; Rare:91 | ||||
| chr6:43687757-43687831 | Common:1; Rare:30 | ||||
| chr6:43770081-43770230 | Common:2; Rare:45 | ||||
| chr6:43771938-43771996 | Rare:9 | ||||
| chr6:44126696-44127024 | Common:1; Rare:84 | ||||
| chr6:44127351-44127639 | Common:4; Rare:81 | ||||
| chr6:44223453-44223841 | Common:2; Rare:113 | ||||
| chr6:44246880-44247193 | Common:4; Rare:132 | ||||
| chr6:44387449-44387782 | Common:4; Rare:89 | ||||
| chr6:46129774-46130171 | Common:5; Rare:126 | ||||
| chr6:46491941-46492037 | Rare:16 | ||||
| chr6:46652688-46653013 | Rare:81 | ||||
| chr6:46921862-46922089 | Common:2; Rare:60 | ||||
| chr6:47477701-47478047 | Common:2; Rare:85; Clinvar:3; Clinvar (benign):3 | ||||
| chr6:47478067-47478247 | Common:2; Rare:67; Clinvar:2; Clinvar (benign):3 |