| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:139028632-139028875 | Common:1; Rare:52 | ||||
| chr6:139374494-139374764 | Common:1; Rare:109 | ||||
| chr6:142147140-142147290 | Rare:56 | ||||
| chr6:142301896-142302124 | Common:5; Rare:66 | ||||
| chr6:143060768-143060926 | Common:6; Rare:60 | ||||
| chr6:143450660-143450936 | Common:1; Rare:103; Clinvar:4; Clinvar (benign):1 | ||||
| chr6:143511651-143511834 | Common:4; Rare:43 | ||||
| chr6:143843247-143843398 | Common:2; Rare:48 | ||||
| chr6:144095501-144095840 | Common:6; Rare:101 | ||||
| chr6:145814680-145814926 | Common:1; Rare:115 | ||||
| chr6:145964255-145964560 | Common:1; Rare:102 | ||||
| chr6:146027621-146027722 | Rare:15 | ||||
| chr6:147508428-147508699 | Common:4; Rare:96 | ||||
| chr6:149545989-149546135 | Rare:62 | ||||
| chr6:149648631-149648836 | Common:1; Rare:64 |