Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:99620394-99620776 | Common:2; Rare:98 | ||||
chr10:99659239-99659574 | Common:2; Rare:86 | ||||
chr10:99731977-99732396 | Common:1; Rare:159; Clinvar:6; Clinvar (benign):1 | ||||
chr10:99732425-99732705 | Common:4; Rare:63; Clinvar:3; Clinvar (benign):2 | ||||
chr10:99782531-99782890 | Common:1; Rare:63; Clinvar:2; Clinvar (benign):1 | ||||
chr10:100185932-100186098 | Rare:66 | ||||
chr10:100229446-100229660 | Rare:78 | ||||
chr10:100267577-100267825 | Common:4; Rare:77 | ||||
chr10:100286596-100286751 | Common:5; Rare:86 | ||||
chr10:100347156-100347529 | Common:4; Rare:86 | ||||
chr10:100912770-100913020 | Common:1; Rare:73 | ||||
chr10:100913328-100913377 | Rare:18 | ||||
chr10:100987218-100987861 | Common:2; Rare:192; Clinvar:3; Clinvar (benign):2 | ||||
chr10:100987864-100987954 | Rare:10; Clinvar (benign):2 | ||||
chr10:101031113-101031302 | Common:1; Rare:40 |