| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:2903306-2903376 | Common:2; Rare:15 | ||||
| chr6:2971190-2971458 | Common:4; Rare:61 | ||||
| chr6:2988628-2988679 | Common:1; Rare:9 | ||||
| chr6:3068496-3068585 | Common:1; Rare:25 | ||||
| chr6:3118567-3118741 | Common:2; Rare:56 | ||||
| chr6:3456027-3456155 | Rare:38 | ||||
| chr6:3456170-3456187 | Rare:3 | ||||
| chr6:3849163-3849422 | Common:3; Rare:70 | ||||
| chr6:4021200-4021428 | Rare:102 | ||||
| chr6:5003656-5003823 | Common:5; Rare:48 | ||||
| chr6:5004007-5004066 | Rare:30 | ||||
| chr6:5260696-5261025 | Common:3; Rare:108; Clinvar (benign):4 | ||||
| chr6:5261245-5261553 | Common:9; Rare:77 | ||||
| chr6:7108546-7108665 | Common:1; Rare:41 | ||||
| chr6:7313055-7313298 | Common:5; Rare:96 |