Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:68956093-68956441 | Common:3; Rare:112 | ||||
chr10:68956601-68956695 | Rare:20 | ||||
chr10:68988506-68988856 | Common:1; Rare:79; Clinvar (benign):2 | ||||
chr10:68988963-68989114 | Common:1; Rare:49; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr10:68989248-68989272 | Rare:8 | ||||
chr10:69087910-69088234 | Rare:74 | ||||
chr10:69179920-69180342 | Common:3; Rare:140 | ||||
chr10:69318573-69318921 | Common:5; Rare:98 | ||||
chr10:70132732-70132822 | Rare:32 | ||||
chr10:70146607-70146869 | Common:1; Rare:74 | ||||
chr10:70170414-70170702 | Common:4; Rare:94 | ||||
chr10:70233300-70233682 | Common:6; Rare:123; Clinvar (benign):1 | ||||
chr10:70816207-70816454 | Common:1; Rare:49 | ||||
chr10:70888214-70888273 | Rare:14 | ||||
chr10:71773417-71773745 | Common:5; Rare:98 |