| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:56620831-56621017 | Rare:38 | ||||
| chr6:56622214-56622310 | Rare:21 | ||||
| chr6:56623643-56623956 | Common:2; Rare:46 | ||||
| chr6:56623977-56624673 | Common:5; Rare:148; Clinvar:2; Clinvar (benign):5 | ||||
| chr6:56625486-56625661 | Common:2; Rare:38 | ||||
| chr6:56627167-56627316 | Rare:37; Clinvar:1; Clinvar (benign):1 | ||||
| chr6:56630383-56630417 | Rare:11 | ||||
| chr6:56630556-56630768 | Rare:37 | ||||
| chr6:56634514-56635126 | Common:2; Rare:124; Clinvar:2; Clinvar (benign):3 | ||||
| chr6:56637317-56637616 | Common:1; Rare:55 | ||||
| chr6:56638139-56638223 | Rare:13 | ||||
| chr6:56638252-56638556 | Common:1; Rare:53 | ||||
| chr6:56660129-56660268 | Rare:23 | ||||
| chr6:56697105-56697411 | Common:1; Rare:53 | ||||
| chr6:56800724-56801019 | Common:4; Rare:66 |