| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:139135114-139135977 | Common:7; Rare:260 | ||||
| chr6:139291993-139292134 | Common:9; Rare:33 | ||||
| chr6:139374609-139374755 | Common:1; Rare:59 | ||||
| chr6:142146993-142147311 | Common:3; Rare:114 | ||||
| chr6:142944990-142945420 | Common:1; Rare:119 | ||||
| chr6:142945456-142946095 | Common:2; Rare:252 | ||||
| chr6:143060568-143060911 | Common:12; Rare:114 | ||||
| chr6:143450011-143450411 | Rare:81 | ||||
| chr6:143450589-143450944 | Common:1; Rare:129; Clinvar:4; Clinvar (benign):1 | ||||
| chr6:143510980-143511560 | Rare:134; Clinvar:1 | ||||
| chr6:143511657-143511866 | Common:4; Rare:48 | ||||
| chr6:143537190-143537660 | Common:4; Rare:113 | ||||
| chr6:143677743-143678036 | Common:2; Rare:63 | ||||
| chr6:143678170-143678610 | Common:2; Rare:94 | ||||
| chr6:143842848-143842982 | Common:1; Rare:27 |