Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:70404485-70404542 | Rare:17 | ||||
chr10:70478663-70478989 | Rare:105 | ||||
chr10:70602708-70602967 | Common:1; Rare:39; Clinvar:1 | ||||
chr10:70815778-70816021 | Common:1; Rare:91 | ||||
chr10:70888530-70888765 | Common:2; Rare:68; Clinvar:5; Clinvar (benign):2 | ||||
chr10:71773417-71773751 | Common:5; Rare:98 | ||||
chr10:71819029-71819417 | Common:1; Rare:85; Clinvar (benign):2 | ||||
chr10:71819463-71819902 | Common:1; Rare:173; Clinvar:5; Clinvar (benign):4 | ||||
chr10:71851181-71851464 | Common:5; Rare:120; Clinvar:4; Clinvar (benign):8; Clinvar (pathogenic):1 | ||||
chr10:72216224-72216318 | Rare:46 | ||||
chr10:72273655-72273988 | Rare:99 | ||||
chr10:72354871-72355196 | Common:2; Rare:116 | ||||
chr10:73096804-73097028 | Common:3; Rare:69 | ||||
chr10:73110481-73110522 | Rare:10 | ||||
chr10:73167916-73168150 | Rare:58 |