| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:143450654-143450934 | Common:1; Rare:104; Clinvar:4; Clinvar (benign):1 | ||||
| chr6:144095524-144095828 | Common:6; Rare:90 | ||||
| chr6:144286142-144286366 | Common:3; Rare:44 | ||||
| chr6:145814735-145814915 | Common:1; Rare:88 | ||||
| chr6:148272186-148272352 | Rare:33 | ||||
| chr6:149546010-149546141 | Rare:55 | ||||
| chr6:149746490-149746666 | Common:3; Rare:89 | ||||
| chr6:149749523-149749805 | Rare:124 | ||||
| chr6:149941835-149942064 | Common:7; Rare:53 | ||||
| chr6:150865656-150865980 | Common:3; Rare:78 | ||||
| chr6:150866330-150866567 | Rare:91 | ||||
| chr6:151452022-151452552 | Common:5; Rare:189; Clinvar (benign):3 | ||||
| chr6:152983009-152983266 | Common:2; Rare:80 | ||||
| chr6:153002606-153002838 | Common:3; Rare:89 | ||||
| chr6:153131211-153131491 | Rare:121 |