| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:3231730-3231887 | Rare:25 | ||||
| chr6:3258803-3259121 | Rare:121 | ||||
| chr6:3849091-3849455 | Common:3; Rare:105 | ||||
| chr6:4021200-4021449 | Rare:109 | ||||
| chr6:5004007-5004112 | Common:1; Rare:51 | ||||
| chr6:5260677-5261017 | Common:3; Rare:116; Clinvar (benign):4 | ||||
| chr6:5261275-5261578 | Common:9; Rare:77 | ||||
| chr6:6006835-6007111 | Common:3; Rare:63 | ||||
| chr6:6007497-6007625 | Common:3; Rare:47 | ||||
| chr6:7313135-7313389 | Common:4; Rare:88 | ||||
| chr6:7389748-7390072 | Common:1; Rare:91 | ||||
| chr6:7541390-7541678 | Rare:89; Clinvar (benign):1 | ||||
| chr6:8102514-8102706 | Common:1; Rare:63 | ||||
| chr6:8435469-8435687 | Common:5; Rare:84 | ||||
| chr6:10556169-10556285 | Rare:31; Clinvar:1 |