Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:20486151-20486167 | Rare:8 | ||||
chr1:20486190-20486479 | Rare:70 | ||||
chr1:20486685-20486851 | Common:1; Rare:44 | ||||
chr1:20507670-20507843 | Common:1; Rare:28 | ||||
chr1:20507846-20507963 | Rare:36 | ||||
chr1:20508041-20508294 | Common:4; Rare:82 | ||||
chr1:20633320-20633569 | Rare:73 | ||||
chr1:20633838-20634041 | Common:1; Rare:84; Clinvar (benign):1 | ||||
chr1:20661042-20661079 | Common:1; Rare:9 | ||||
chr1:20661338-20661790 | Common:3; Rare:156; Clinvar:4; Clinvar (benign):6 | ||||
chr1:20661853-20661924 | Rare:18 | ||||
chr1:20731572-20731756 | Common:2; Rare:42 | ||||
chr1:20732139-20732745 | Common:3; Rare:127 | ||||
chr1:20732773-20733403 | Common:7; Rare:127 | ||||
chr1:20785941-20786052 | Rare:21 |