Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr15:88913263-88913410 | Common:3; Rare:46 | ||||
chr15:89243938-89244008 | Rare:23; Clinvar:2 | ||||
chr15:89321189-89321502 | Common:3; Rare:93; Clinvar:6; Clinvar (benign):8; Clinvar (pathogenic):4 | ||||
chr15:89334799-89335069 | Common:3; Rare:100 | ||||
chr15:89480092-89480436 | Common:1; Rare:101 | ||||
chr15:89496314-89496714 | Common:2; Rare:144 | ||||
chr15:89679302-89679540 | Common:1; Rare:43 | ||||
chr15:89893960-89894142 | Common:3; Rare:60 | ||||
chr15:90184853-90184951 | Common:1; Rare:24 | ||||
chr15:90233881-90234246 | Common:6; Rare:101 | ||||
chr15:90473776-90474099 | Common:2; Rare:101 | ||||
chr15:90529824-90530016 | Common:3; Rare:72 | ||||
chr15:90994496-90994742 | Common:1; Rare:82 | ||||
chr15:92904235-92904583 | Common:3; Rare:150 | ||||
chr15:94231414-94231604 | Common:1; Rare:65 |