| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:142309380-142310030 | Common:4; Rare:205; Clinvar (pathogenic):2 | ||||
| chr6:142331063-142331458 | Common:6; Rare:142 | ||||
| chr6:142377203-142377603 | Common:2; Rare:93 | ||||
| chr6:142845190-142846201 | Common:8; Rare:287 | ||||
| chr6:142926670-142927077 | Common:5; Rare:144 | ||||
| chr6:142946265-142946500 | Common:4; Rare:98 | ||||
| chr6:143061537-143061980 | Common:6; Rare:118 | ||||
| chr6:143745390-143745820 | Common:4; Rare:161 | ||||
| chr6:144286211-144286552 | Common:6; Rare:111 | ||||
| chr6:144302601-144303110 | Common:11; Rare:194 | ||||
| chr6:144370801-144371350 | Common:3; Rare:123 | ||||
| chr6:144661360-144661660 | Rare:56 | ||||
| chr6:145267098-145267710 | Common:7; Rare:148 | ||||
| chr6:147203682-147203807 | Common:1; Rare:60 | ||||
| chr6:147660556-147660732 | Common:2; Rare:54 |