| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:2999613-2999999 | Common:10; Rare:82 | ||||
| chr6:3068520-3068592 | Common:1; Rare:20 | ||||
| chr6:3118366-3118764 | Common:5; Rare:133 | ||||
| chr6:3157530-3157670 | Common:6; Rare:52 | ||||
| chr6:3283861-3284193 | Common:3; Rare:90 | ||||
| chr6:3751339-3751377 | Rare:9 | ||||
| chr6:4021187-4021445 | Rare:113 | ||||
| chr6:5004007-5004108 | Common:1; Rare:49 | ||||
| chr6:5260737-5261025 | Common:2; Rare:91; Clinvar (benign):2 | ||||
| chr6:5261238-5261554 | Common:9; Rare:79 | ||||
| chr6:7108559-7108824 | Common:5; Rare:90 | ||||
| chr6:7313082-7313380 | Common:5; Rare:112 | ||||
| chr6:7389740-7390072 | Common:1; Rare:96 | ||||
| chr6:7541375-7541770 | Common:1; Rare:120; Clinvar:2; Clinvar (benign):1 | ||||
| chr6:7541786-7541832 | Common:1; Rare:9 |