Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:70382534-70382872 | Common:5; Rare:131 | ||||
chr10:70403939-70404286 | Common:1; Rare:115 | ||||
chr10:70404441-70404588 | Common:1; Rare:52 | ||||
chr10:70672316-70672624 | Common:2; Rare:80 | ||||
chr10:70815778-70816117 | Common:1; Rare:109 | ||||
chr10:70816176-70816632 | Common:1; Rare:89 | ||||
chr10:70888190-70888352 | Common:3; Rare:35 | ||||
chr10:70888354-70888731 | Common:3; Rare:100; Clinvar:5; Clinvar (benign):2 | ||||
chr10:71212355-71212794 | Common:2; Rare:125 | ||||
chr10:71319162-71319328 | Common:2; Rare:59; Clinvar:2; Clinvar (benign):1 | ||||
chr10:71319603-71319769 | Common:2; Rare:38 | ||||
chr10:71712998-71713150 | Common:2; Rare:47 | ||||
chr10:71773496-71773715 | Common:3; Rare:65 | ||||
chr10:71850735-71850899 | Rare:38 | ||||
chr10:71851011-71851095 | Rare:29 |