Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:179882493-179882887 | Rare:196; Clinvar:9; Clinvar (benign):2 | ||||
chr1:179883007-179883153 | Common:3; Rare:57 | ||||
chr1:179954456-179954817 | Common:3; Rare:88 | ||||
chr1:180154685-180154904 | Common:1; Rare:79 | ||||
chr1:181088494-181088704 | Rare:67 | ||||
chr1:182789655-182789778 | Common:2; Rare:40 | ||||
chr1:182839198-182839449 | Common:1; Rare:102 | ||||
chr1:182839540-182839751 | Common:2; Rare:91 | ||||
chr1:183186166-183186335 | Common:3; Rare:34; Clinvar:1; Clinvar (benign):3 | ||||
chr1:183472320-183472522 | Common:2; Rare:68 | ||||
chr1:183635660-183636114 | Common:5; Rare:127 | ||||
chr1:184051617-184051938 | Common:4; Rare:117 | ||||
chr1:184754598-184754683 | Common:1; Rare:40 | ||||
chr1:184974391-184974617 | Rare:58 | ||||
chr1:185045229-185045637 | Common:2; Rare:143 |