Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:42654666-42654868 | Rare:44 | ||||
chr10:46786688-46786759 | Rare:11 | ||||
chr10:46786803-46786900 | Rare:6 | ||||
chr10:47553472-47553594 | Rare:13 | ||||
chr10:61903005-61903348 | Common:1; Rare:91 | ||||
chr10:73126205-73126399 | Common:1; Rare:40 | ||||
chr10:73247212-73247370 | Rare:86 | ||||
chr10:73730452-73730595 | Common:1; Rare:38 | ||||
chr10:79826315-79826678 | Common:4; Rare:99 | ||||
chr10:79904933-79905048 | Common:3; Rare:23 | ||||
chr10:80536013-80536102 | Common:4; Rare:24 | ||||
chr10:86955638-86955780 | Rare:24 | ||||
chr10:86971194-86971428 | Common:2; Rare:80 | ||||
chr10:87342316-87342942 | Common:5; Rare:192 | ||||
chr10:88939627-88939820 | Rare:32; Clinvar:1; Clinvar (benign):1 |