Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:149927757-149927900 | Common:1; Rare:60; Clinvar (benign):5 | ||||
chr1:150067131-150067311 | Common:3; Rare:33 | ||||
chr1:150067651-150067866 | Rare:65 | ||||
chr1:150234676-150234693 | Rare:1 | ||||
chr1:150268353-150268487 | Rare:26 | ||||
chr1:150282285-150282586 | Common:3; Rare:59 | ||||
chr1:150321406-150321608 | Rare:63; Clinvar:3; Clinvar (benign):1 | ||||
chr1:150363957-150364232 | Common:3; Rare:97 | ||||
chr1:150364584-150364762 | Rare:63 | ||||
chr1:150487233-150487447 | Common:4; Rare:49; Clinvar (benign):3 | ||||
chr1:150549202-150549434 | Rare:61 | ||||
chr1:150579196-150579271 | Rare:33 | ||||
chr1:150579595-150579873 | Common:10; Rare:90 | ||||
chr1:150629107-150629369 | Common:1; Rare:73 | ||||
chr1:150629421-150629816 | Rare:90 |