| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:143450654-143450944 | Common:1; Rare:107; Clinvar:4; Clinvar (benign):1 | ||||
| chr6:143677822-143678135 | Common:2; Rare:75 | ||||
| chr6:143843189-143843398 | Common:2; Rare:65 | ||||
| chr6:144286115-144286332 | Common:3; Rare:38 | ||||
| chr6:145814664-145814955 | Common:1; Rare:134 | ||||
| chr6:145964299-145964561 | Common:1; Rare:89 | ||||
| chr6:149718059-149718151 | Common:1; Rare:30 | ||||
| chr6:149746476-149746642 | Common:2; Rare:81 | ||||
| chr6:149749523-149749805 | Rare:124 | ||||
| chr6:149963834-149964007 | Common:1; Rare:53 | ||||
| chr6:150866311-150866512 | Rare:81 | ||||
| chr6:151391513-151391849 | Common:3; Rare:94 | ||||
| chr6:151452025-151452552 | Common:5; Rare:186; Clinvar (benign):2 | ||||
| chr6:152983009-152983260 | Common:2; Rare:79 | ||||
| chr6:152983518-152983759 | Common:4; Rare:92 |