Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:98268190-98268480 | Common:3; Rare:74 | ||||
chr10:98446870-98447055 | Rare:53 | ||||
chr10:99235957-99236035 | Common:5; Rare:22 | ||||
chr10:99430621-99430957 | Common:3; Rare:81 | ||||
chr10:99659265-99659547 | Common:1; Rare:70 | ||||
chr10:99732076-99732331 | Rare:93; Clinvar:3 | ||||
chr10:100185926-100186190 | Rare:104 | ||||
chr10:100267616-100267986 | Common:9; Rare:100 | ||||
chr10:100286623-100286717 | Common:2; Rare:61 | ||||
chr10:100346911-100347272 | Common:1; Rare:86 | ||||
chr10:100912751-100912981 | Common:1; Rare:70 | ||||
chr10:100913335-100913355 | Rare:7 | ||||
chr10:100987405-100987571 | Common:1; Rare:67; Clinvar:1; Clinvar (benign):1 | ||||
chr10:100997020-100997124 | Rare:33 | ||||
chr10:101031102-101031275 | Common:1; Rare:41 |