Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:45465269-45465352 | Common:1; Rare:17 | ||||
chr13:46052418-46052493 | Rare:21 | ||||
chr13:46052627-46052821 | Common:2; Rare:49 | ||||
chr13:46182130-46182430 | Common:3; Rare:51 | ||||
chr13:46211814-46212034 | Common:2; Rare:67 | ||||
chr13:46797117-46797306 | Common:3; Rare:72 | ||||
chr13:48037652-48037761 | Rare:52 | ||||
chr13:48303645-48304031 | Common:1; Rare:130; Clinvar:15; Clinvar (benign):7; Clinvar (pathogenic):2 | ||||
chr13:48653820-48653952 | Rare:24 | ||||
chr13:49247740-49248091 | Common:1; Rare:94 | ||||
chr13:49248253-49248333 | Rare:18 | ||||
chr13:49443997-49444476 | Common:1; Rare:156 | ||||
chr13:49585481-49585611 | Common:1; Rare:42 | ||||
chr13:49792512-49792868 | Common:6; Rare:138 | ||||
chr13:49936296-49936569 | Rare:78 |