Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:99659265-99659554 | Common:1; Rare:70 | ||||
chr10:99732070-99732332 | Rare:97; Clinvar:4; Clinvar (benign):1 | ||||
chr10:100009862-100010080 | Common:1; Rare:67 | ||||
chr10:100185895-100186198 | Rare:113 | ||||
chr10:100229553-100229657 | Rare:33 | ||||
chr10:100286642-100286730 | Common:2; Rare:47 | ||||
chr10:100346921-100347283 | Common:1; Rare:85 | ||||
chr10:100912772-100913039 | Common:1; Rare:78 | ||||
chr10:100913335-100913461 | Rare:31 | ||||
chr10:100987273-100987598 | Common:1; Rare:120; Clinvar:1; Clinvar (benign):1 | ||||
chr10:100999686-100999952 | Common:1; Rare:75 | ||||
chr10:101031113-101031533 | Common:1; Rare:93 | ||||
chr10:101588147-101588330 | Rare:74 | ||||
chr10:101694896-101695216 | Rare:78; Clinvar:2 | ||||
chr10:101818267-101818762 | Common:1; Rare:134 |