chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8117686058117686059CT48GENIChomozygous52830465
8117687057117687058TC26GENIChomozygous52830466
8117687267117687268AT29GENIChomozygous52830467
8117687282117687283CT28GENIChomozygous52830468
8117687352117687357AAAAA-----10GENICheterozygous53523981
8117687353117687357AAAA----10GENICheterozygous53411688
8117687354117687357AAA---10GENICheterozygous53411689
8117687994117687995CCTCCT4GENIChomozygous52830471
8117688030117688031CCTCCTTCCT20GENIChomozygous53411690
8117688224117688225TTTCTC4GENIChomozygous52830474
8117688547117688548AG19GENIChomozygous52830475
8117688914117688915AG29GENIChomozygous52830476
8117689018117689019CA25GENIChomozygous52830477
8117689210117689212CA--5GENIChomozygous53411692
8117690379117690380AG35GENIChomozygous52830479
8117691256117691257CT38GENIChomozygous52830480
8117692052117692053AC39GENIChomozygous52830481
8117692346117692347AG46GENIChomozygous52830482
8117693958117693959GT19GENIChomozygous52830483
8117693990117693991AG16GENIChomozygous52830484
8117694232117694233AG13GENIChomozygous52830485
8117694329117694330CCAA5GENIChomozygous52830486
8117694337117694338TA6GENIChomozygous53411693
8117694457117694460AAA---14GENIChomozygous52830488
8117695105117695106TC21GENIChomozygous52830490
8117695370117695371AG29GENIChomozygous52830491
8117697157117697173AACCATGCACACCTGT----------------37GENIChomozygous53411695
8117697279117697280AG32GENIChomozygous52830497
8117697841117697842GA22GENIChomozygous52830498
8117698793117698794GGTT15GENIChomozygous52830499
8117699483117699487TTTT----6GENIChomozygous52830500
8117699523117699524GGTTTT4GENIChomozygous52830503
8117699533117699534GT8GENIChomozygous52830506