| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:139374504-139374788 | Common:1; Rare:114 | ||||
| chr6:142089059-142089224 | Common:1; Rare:26 | ||||
| chr6:142147120-142147290 | Common:3; Rare:62 | ||||
| chr6:142945013-142945131 | Rare:42 | ||||
| chr6:142945696-142945981 | Common:1; Rare:64 | ||||
| chr6:143060442-143060494 | Rare:11 | ||||
| chr6:143060724-143060940 | Common:7; Rare:78 | ||||
| chr6:143450660-143450936 | Common:1; Rare:103; Clinvar:4; Clinvar (benign):1 | ||||
| chr6:143511632-143511779 | Common:4; Rare:36 | ||||
| chr6:144583152-144583501 | Common:1; Rare:64 | ||||
| chr6:145734753-145734894 | Common:3; Rare:48 | ||||
| chr6:145814685-145814926 | Common:1; Rare:114 | ||||
| chr6:145964266-145964490 | Common:1; Rare:75 | ||||
| chr6:146027523-146027724 | Common:1; Rare:38 | ||||
| chr6:147508421-147508716 | Common:5; Rare:102 |