Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:74176423-74176569 | Rare:34 | ||||
chr10:74176636-74176730 | Rare:25; Clinvar:1 | ||||
chr10:74176732-74176806 | Rare:22; Clinvar:2 | ||||
chr10:75111565-75111666 | Rare:25 | ||||
chr10:75210480-75210867 | Common:1; Rare:129 | ||||
chr10:78029466-78029643 | Common:1; Rare:53; Clinvar (benign):1 | ||||
chr10:80205481-80205693 | Common:4; Rare:78 | ||||
chr10:84139286-84139593 | Common:4; Rare:82 | ||||
chr10:87094912-87095235 | Common:1; Rare:78; Clinvar:2 | ||||
chr10:87504808-87504879 | Common:1; Rare:19 | ||||
chr10:87818144-87818355 | Common:1; Rare:76 | ||||
chr10:88880152-88880529 | Rare:81 | ||||
chr10:88990690-88990804 | Common:1; Rare:31; Clinvar (benign):1 | ||||
chr10:88991343-88991442 | Common:2; Rare:16 | ||||
chr10:89643886-89644181 | Rare:64 |