| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:139291946-139292339 | Common:10; Rare:74 | ||||
| chr6:142147120-142147290 | Common:3; Rare:62 | ||||
| chr6:143060724-143060942 | Common:7; Rare:78 | ||||
| chr6:143450660-143450931 | Common:1; Rare:101; Clinvar:4; Clinvar (benign):1 | ||||
| chr6:143678098-143678196 | Rare:24 | ||||
| chr6:144286141-144286366 | Common:3; Rare:44 | ||||
| chr6:145814666-145814921 | Common:1; Rare:114 | ||||
| chr6:147204394-147204425 | Rare:9 | ||||
| chr6:149546003-149546249 | Common:1; Rare:104 | ||||
| chr6:149749523-149749811 | Rare:126 | ||||
| chr6:151240237-151240436 | Common:1; Rare:54 | ||||
| chr6:151325426-151325727 | Common:2; Rare:70 | ||||
| chr6:151452034-151452584 | Common:4; Rare:196 | ||||
| chr6:152302080-152302213 | Rare:41 | ||||
| chr6:152983022-152983266 | Common:2; Rare:76 |