| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:33454389-33454604 | Rare:63 | ||||
| chr6:33580180-33580376 | Common:2; Rare:55 | ||||
| chr6:34236752-34236914 | Common:2; Rare:64 | ||||
| chr6:34248494-34248581 | Rare:12 | ||||
| chr6:34248972-34249230 | Rare:57 | ||||
| chr6:34392268-34392892 | Common:2; Rare:218 | ||||
| chr6:34425831-34426184 | Common:6; Rare:121; Clinvar:1; Clinvar (benign):8 | ||||
| chr6:34696734-34697085 | Common:1; Rare:77 | ||||
| chr6:34757285-34757550 | Common:2; Rare:73 | ||||
| chr6:34791980-34792130 | Common:3; Rare:46 | ||||
| chr6:34887953-34888102 | Common:1; Rare:40 | ||||
| chr6:35259427-35259778 | Common:3; Rare:109 | ||||
| chr6:35468231-35468472 | Common:3; Rare:95 | ||||
| chr6:35921047-35921181 | Rare:68 | ||||
| chr6:36442900-36443087 | Common:2; Rare:77 |