| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:87155243-87155614 | Rare:101 | ||||
| chr6:87472890-87473006 | Common:1; Rare:44; Clinvar (benign):4 | ||||
| chr6:87589955-87590186 | Common:3; Rare:108; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr6:87702218-87702485 | Common:1; Rare:82 | ||||
| chr6:88963517-88963850 | Common:2; Rare:107 | ||||
| chr6:89080581-89080777 | Common:1; Rare:86 | ||||
| chr6:89145983-89146090 | Rare:32 | ||||
| chr6:89412072-89412356 | Common:3; Rare:68 | ||||
| chr6:89638404-89638549 | Common:1; Rare:32 | ||||
| chr6:89638705-89638845 | Common:4; Rare:49 | ||||
| chr6:89819699-89819888 | Rare:64 | ||||
| chr6:89829594-89829964 | Rare:98 | ||||
| chr6:90586991-90587337 | Common:3; Rare:95 | ||||
| chr6:93419546-93419831 | Common:1; Rare:76 | ||||
| chr6:95577347-95577578 | Common:6; Rare:65 |