| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:42929193-42929406 | Common:3; Rare:52 | ||||
| chr6:42929421-42929550 | Common:1; Rare:41 | ||||
| chr6:42979162-42979303 | Common:2; Rare:43; Clinvar:4; Clinvar (benign):1 | ||||
| chr6:42984281-42984592 | Rare:74 | ||||
| chr6:43013872-43014329 | Common:2; Rare:100 | ||||
| chr6:43059820-43059905 | Rare:28 | ||||
| chr6:43075965-43076315 | Rare:102 | ||||
| chr6:43427321-43427599 | Common:1; Rare:57 | ||||
| chr6:43477493-43477626 | Rare:35 | ||||
| chr6:43516800-43517112 | Common:5; Rare:113; Clinvar:2; Clinvar (benign):1 | ||||
| chr6:43575948-43576161 | Rare:82; Clinvar:2 | ||||
| chr6:43635755-43635881 | Common:1; Rare:31 | ||||
| chr6:44127369-44127624 | Common:4; Rare:70 | ||||
| chr6:44223474-44223615 | Common:1; Rare:44 | ||||
| chr6:44387452-44387749 | Common:4; Rare:77 |