Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:100185914-100186194 | Rare:110 | ||||
chr10:100229503-100229704 | Common:1; Rare:74 | ||||
chr10:100267597-100267746 | Common:3; Rare:49 | ||||
chr10:100286335-100286726 | Common:4; Rare:138 | ||||
chr10:100346923-100347438 | Common:3; Rare:118 | ||||
chr10:100347456-100347595 | Common:2; Rare:48 | ||||
chr10:100529836-100529955 | Rare:35 | ||||
chr10:100535877-100536255 | Common:6; Rare:135 | ||||
chr10:100912730-100913023 | Common:1; Rare:93 | ||||
chr10:100913328-100913436 | Rare:30 | ||||
chr10:100987180-100987662 | Common:2; Rare:163; Clinvar:1; Clinvar (benign):2 | ||||
chr10:100999254-100999324 | Rare:13 | ||||
chr10:101031102-101031275 | Common:1; Rare:41 | ||||
chr10:101353760-101354220 | Common:1; Rare:141 | ||||
chr10:101354366-101354633 | Common:1; Rare:67 |