| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:85643817-85643964 | Common:2; Rare:44 | ||||
| chr6:87155212-87155601 | Rare:104 | ||||
| chr6:87589946-87590164 | Common:2; Rare:99; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr6:87701710-87701713 | |||||
| chr6:87702189-87702534 | Common:2; Rare:109 | ||||
| chr6:88165868-88166337 | Common:3; Rare:143 | ||||
| chr6:88963490-88963773 | Rare:91 | ||||
| chr6:89080571-89080768 | Common:1; Rare:84 | ||||
| chr6:89117937-89118133 | Common:4; Rare:82 | ||||
| chr6:89412072-89412409 | Common:3; Rare:77 | ||||
| chr6:89638443-89638591 | Common:1; Rare:30 | ||||
| chr6:89638721-89638845 | Common:3; Rare:42 | ||||
| chr6:89819702-89819874 | Rare:58 | ||||
| chr6:89829566-89829964 | Rare:107 | ||||
| chr6:90296566-90296936 | Common:4; Rare:121 |