Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:26748678-26748863 | Common:4; Rare:45 | ||||
chr10:26760534-26760573 | Rare:4 | ||||
chr10:26763463-26763619 | Common:3; Rare:30 | ||||
chr10:26764924-26764971 | Common:1; Rare:11 | ||||
chr10:27045157-27045419 | Common:1; Rare:60 | ||||
chr10:27051838-27051927 | Common:1; Rare:8 | ||||
chr10:27065759-27065848 | Rare:15 | ||||
chr10:27093429-27093759 | Common:5; Rare:100; Clinvar (benign):1 | ||||
chr10:27116057-27116279 | Common:2; Rare:41 | ||||
chr10:27122962-27122983 | Rare:1 | ||||
chr10:27130471-27130612 | Common:2; Rare:22 | ||||
chr10:27131629-27131938 | Rare:54 | ||||
chr10:27144861-27145126 | Common:2; Rare:60 | ||||
chr10:27513867-27513982 | Common:2; Rare:21 | ||||
chr10:27526578-27526889 | Common:1; Rare:56 |