| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:85643808-85643921 | Common:2; Rare:34 | ||||
| chr6:87155248-87155618 | Rare:103 | ||||
| chr6:87472894-87473004 | Common:1; Rare:42; Clinvar (benign):4 | ||||
| chr6:87518604-87518834 | Common:1; Rare:70; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):5 | ||||
| chr6:87589955-87590177 | Common:3; Rare:102; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr6:87701460-87701645 | Common:1; Rare:67 | ||||
| chr6:88963561-88963830 | Common:2; Rare:92 | ||||
| chr6:89145925-89146132 | Rare:62 | ||||
| chr6:89352704-89352988 | Common:1; Rare:64 | ||||
| chr6:89638447-89638521 | Common:1; Rare:15 | ||||
| chr6:89638702-89638824 | Common:4; Rare:45 | ||||
| chr6:89819709-89819882 | Rare:59 | ||||
| chr6:89829595-89830062 | Common:2; Rare:117 | ||||
| chr6:90586995-90587357 | Common:4; Rare:103 | ||||
| chr6:93419546-93419783 | Common:1; Rare:65 |