| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:3118365-3118755 | Common:5; Rare:129 | ||||
| chr6:3157520-3157683 | Common:6; Rare:58 | ||||
| chr6:3456141-3456188 | Rare:13 | ||||
| chr6:4021161-4021460 | Rare:124 | ||||
| chr6:4135225-4135324 | Common:1; Rare:28 | ||||
| chr6:4135488-4135616 | Common:5; Rare:71 | ||||
| chr6:5003662-5003830 | Common:5; Rare:49 | ||||
| chr6:5004007-5004115 | Common:1; Rare:52 | ||||
| chr6:5260681-5261017 | Common:3; Rare:114; Clinvar (benign):4 | ||||
| chr6:5261275-5261585 | Common:9; Rare:83 | ||||
| chr6:7107920-7108036 | Rare:24 | ||||
| chr6:7108229-7108519 | Rare:89 | ||||
| chr6:7108553-7108684 | Common:1; Rare:44 | ||||
| chr6:7108785-7108872 | Common:1; Rare:23 | ||||
| chr6:7313052-7313380 | Common:5; Rare:124 |