| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:33454368-33454693 | Common:1; Rare:89 | ||||
| chr6:33711380-33711507 | Common:1; Rare:44 | ||||
| chr6:33711631-33711811 | Common:1; Rare:69; Clinvar (benign):1 | ||||
| chr6:33788463-33788688 | Common:1; Rare:58 | ||||
| chr6:33789108-33789206 | Rare:58 | ||||
| chr6:34236749-34236906 | Common:3; Rare:65 | ||||
| chr6:34248977-34249262 | Common:1; Rare:62 | ||||
| chr6:34392265-34392887 | Common:1; Rare:219 | ||||
| chr6:34425964-34426143 | Common:4; Rare:80; Clinvar:1; Clinvar (benign):8 | ||||
| chr6:34696506-34697049 | Common:1; Rare:137 | ||||
| chr6:34757357-34757586 | Common:1; Rare:72 | ||||
| chr6:34791903-34792149 | Common:4; Rare:77 | ||||
| chr6:34887859-34888111 | Common:1; Rare:76 | ||||
| chr6:34889143-34889599 | Common:6; Rare:114 | ||||
| chr6:35140928-35140969 | Rare:8 |