| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:693061-693194 | Rare:43 | ||||
| chr6:2971269-2971571 | Common:4; Rare:73 | ||||
| chr6:2999644-2999893 | Common:10; Rare:51 | ||||
| chr6:3118602-3118743 | Common:2; Rare:47 | ||||
| chr6:3157541-3157662 | Common:6; Rare:45 | ||||
| chr6:4021209-4021422 | Rare:99 | ||||
| chr6:5004007-5004102 | Common:1; Rare:48 | ||||
| chr6:5260719-5261025 | Common:2; Rare:96; Clinvar (benign):2 | ||||
| chr6:5261268-5261563 | Common:9; Rare:76 | ||||
| chr6:7313127-7313383 | Common:4; Rare:93 | ||||
| chr6:7389676-7389976 | Common:2; Rare:90 | ||||
| chr6:7541366-7541684 | Common:1; Rare:94; Clinvar (benign):1 | ||||
| chr6:7541845-7542035 | Common:2; Rare:78; Clinvar:11; Clinvar (benign):8; Clinvar (pathogenic):1 | ||||
| chr6:8435361-8435659 | Common:4; Rare:105 | ||||
| chr6:10521208-10521355 | Rare:38 |