Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:22927989-22928084 | Common:1; Rare:34 | ||||
chr10:24623139-24623254 | Rare:19 | ||||
chr10:24722667-24722832 | Rare:41 | ||||
chr10:24952288-24952368 | Rare:15 | ||||
chr10:25016445-25016692 | Common:6; Rare:100 | ||||
chr10:26438051-26438364 | Common:2; Rare:73 | ||||
chr10:27100398-27100591 | Common:3; Rare:57; Clinvar:4; Clinvar (benign):2 | ||||
chr10:27154315-27154456 | Rare:38 | ||||
chr10:27155181-27155397 | Common:4; Rare:82; Clinvar:4; Clinvar (benign):4 | ||||
chr10:27240478-27240547 | Rare:28 | ||||
chr10:27240575-27240896 | Common:2; Rare:84 | ||||
chr10:27242058-27242235 | Common:1; Rare:76 | ||||
chr10:28532486-28532862 | Common:5; Rare:149 | ||||
chr10:28677245-28677521 | Common:5; Rare:127 | ||||
chr10:29735772-29736037 | Common:3; Rare:53 |