Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:97445983-97446217 | Rare:60 | ||||
chr10:97737031-97737146 | Rare:39 | ||||
chr10:98446850-98446899 | Rare:15; Clinvar:1 | ||||
chr10:99430611-99430940 | Common:3; Rare:75 | ||||
chr10:99659273-99659529 | Common:1; Rare:64 | ||||
chr10:99732070-99732312 | Rare:88; Clinvar:4; Clinvar (benign):1 | ||||
chr10:100185907-100186184 | Rare:106 | ||||
chr10:100346938-100347363 | Common:1; Rare:99 | ||||
chr10:100912675-100913039 | Common:1; Rare:108 | ||||
chr10:100987256-100987584 | Common:1; Rare:119; Clinvar:1; Clinvar (benign):1 | ||||
chr10:100997960-100998279 | Common:1; Rare:66 | ||||
chr10:101031093-101031264 | Common:1; Rare:42 | ||||
chr10:101229445-101229573 | Rare:26 | ||||
chr10:101588211-101588338 | Rare:51 | ||||
chr10:101818372-101818762 | Common:1; Rare:102 |