| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:133952931-133953248 | Common:2; Rare:83 | ||||
| chr6:134174840-134175029 | Common:1; Rare:92 | ||||
| chr6:134177843-134178091 | Common:1; Rare:37 | ||||
| chr6:135054784-135054962 | Common:6; Rare:52 | ||||
| chr6:135497588-135497880 | Common:4; Rare:107; Clinvar:2; Clinvar (benign):2 | ||||
| chr6:136289338-136289440 | Rare:50 | ||||
| chr6:136289767-136290063 | Common:2; Rare:132 | ||||
| chr6:136550409-136550659 | Common:2; Rare:70 | ||||
| chr6:137219279-137219443 | Common:2; Rare:62; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr6:137866968-137867277 | Rare:72 | ||||
| chr6:138107245-138107622 | Common:5; Rare:117 | ||||
| chr6:138404246-138404563 | Common:6; Rare:89 | ||||
| chr6:138545663-138545769 | Rare:25 | ||||
| chr6:138773646-138773833 | Common:3; Rare:87 | ||||
| chr6:139028553-139028827 | Common:1; Rare:54 |