| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:37433166-37433297 | Common:2; Rare:35 | ||||
| chr6:38639810-38640208 | Rare:99 | ||||
| chr6:39934447-39934773 | Common:3; Rare:111 | ||||
| chr6:41072318-41072981 | Rare:192 | ||||
| chr6:41546143-41546409 | Common:1; Rare:71 | ||||
| chr6:41921079-41921544 | Common:3; Rare:122 | ||||
| chr6:42452181-42452357 | Common:1; Rare:38 | ||||
| chr6:42746071-42746348 | Rare:77 | ||||
| chr6:42879594-42879673 | Rare:22 | ||||
| chr6:42929092-42929185 | Rare:26 | ||||
| chr6:42929209-42929797 | Common:6; Rare:199 | ||||
| chr6:42984297-42984631 | Rare:84 | ||||
| chr6:43013862-43014304 | Common:2; Rare:102 | ||||
| chr6:43053772-43054017 | Common:2; Rare:77; Clinvar:5; Clinvar (benign):1 | ||||
| chr6:43059808-43059921 | Rare:37 |