| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:125790780-125791240 | Common:2; Rare:128 | ||||
| chr6:125956619-125956790 | Common:2; Rare:52 | ||||
| chr6:125986317-125986579 | Common:1; Rare:97 | ||||
| chr6:125986751-125987151 | Common:4; Rare:104 | ||||
| chr6:126339974-126340182 | Common:1; Rare:56 | ||||
| chr6:127266497-127266931 | Common:2; Rare:147 | ||||
| chr6:127343257-127343679 | Common:2; Rare:93 | ||||
| chr6:127518758-127519188 | Common:3; Rare:74 | ||||
| chr6:127519191-127519483 | Common:1; Rare:38 | ||||
| chr6:128067051-128067551 | Common:6; Rare:251 | ||||
| chr6:128520365-128520820 | Common:5; Rare:152 | ||||
| chr6:128521019-128521419 | Common:1; Rare:86 | ||||
| chr6:128882888-128883482 | Common:4; Rare:258; Clinvar:14; Clinvar (benign):6; Clinvar (pathogenic):5 | ||||
| chr6:129710160-129710370 | Common:1; Rare:50 | ||||
| chr6:130018456-130018632 | Rare:38 |