| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:2245436-2245825 | Common:1; Rare:133 | ||||
| chr6:2971259-2971714 | Common:5; Rare:116 | ||||
| chr6:2971725-2971864 | Rare:31 | ||||
| chr6:2999584-3000006 | Common:11; Rare:91 | ||||
| chr6:3068525-3068553 | Rare:5 | ||||
| chr6:3118373-3118737 | Common:5; Rare:112 | ||||
| chr6:4021174-4021423 | Rare:109 | ||||
| chr6:5004007-5004106 | Common:1; Rare:49 | ||||
| chr6:5084395-5084737 | Common:3; Rare:84 | ||||
| chr6:5260729-5261051 | Common:4; Rare:110; Clinvar (benign):2 | ||||
| chr6:7108585-7108665 | Rare:28 | ||||
| chr6:7313083-7313385 | Common:5; Rare:112 | ||||
| chr6:7389740-7389875 | Common:1; Rare:40 | ||||
| chr6:7541343-7541770 | Common:2; Rare:127; Clinvar:2; Clinvar (benign):1 | ||||
| chr6:7590072-7590260 | Common:5; Rare:62 |