| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:135054797-135054992 | Common:5; Rare:58 | ||||
| chr6:136289773-136290057 | Common:2; Rare:123 | ||||
| chr6:136526574-136526593 | Rare:2 | ||||
| chr6:143060750-143060910 | Common:6; Rare:57 | ||||
| chr6:143450669-143450899 | Common:1; Rare:91; Clinvar:4; Clinvar (benign):1 | ||||
| chr6:143511652-143511781 | Common:4; Rare:33 | ||||
| chr6:143677843-143678005 | Common:2; Rare:33 | ||||
| chr6:144008236-144008440 | Rare:71 | ||||
| chr6:144285171-144285335 | Common:2; Rare:53 | ||||
| chr6:145814750-145814932 | Common:1; Rare:89 | ||||
| chr6:146543765-146544111 | Common:5; Rare:143 | ||||
| chr6:149863473-149863532 | Rare:12 | ||||
| chr6:149864018-149864112 | Common:2; Rare:26 | ||||
| chr6:153002666-153002841 | Common:3; Rare:58 | ||||
| chr6:154510522-154510826 | Common:2; Rare:95 |