| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:43013908-43014270 | Common:1; Rare:74 | ||||
| chr6:43516859-43517107 | Common:4; Rare:93; Clinvar:2; Clinvar (benign):1 | ||||
| chr6:44127351-44127634 | Common:4; Rare:80 | ||||
| chr6:44387447-44387729 | Common:4; Rare:70 | ||||
| chr6:52995344-52995643 | Common:4; Rare:123 | ||||
| chr6:75243759-75243975 | Common:1; Rare:91 | ||||
| chr6:75284722-75285015 | Common:1; Rare:82 | ||||
| chr6:83193222-83193389 | Common:3; Rare:58 | ||||
| chr6:87589959-87590145 | Common:1; Rare:77; Clinvar (benign):4 | ||||
| chr6:89638732-89638824 | Common:3; Rare:28 | ||||
| chr6:100881281-100881482 | Common:5; Rare:88 | ||||
| chr6:106629463-106629584 | Common:1; Rare:23 | ||||
| chr6:110415542-110415651 | Rare:24 | ||||
| chr6:112087452-112087663 | Rare:65 | ||||
| chr6:116571209-116571568 | Common:2; Rare:100 |