chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
124905051449050515TTC7GENIChomozygous50230908
124905051549050516TTTTCTTTC1GENIChomozygous50575610
124905051949050520AC7GENIChomozygous50575612
124905052349050524AC7GENIChomozygous50230912
124905052749050528AC7GENIChomozygous50230914
124905053149050532AC9GENIChomozygous50230916
124905053549050536AC9GENIChomozygous50230918
124905053949050540AC8GENIChomozygous50230920
124905054349050544AC9GENIChomozygous50230922
124905139449051395CA11GENIChomozygous50230926
124905175549051756GGT5GENICheterozygous50546601
124905176049051761T-5GENICheterozygous50559366
124905205549052056C-16GENICheterozygous50546603
124905230049052301AAGT16GENIChomozygous50230930
124905236449052365AT24GENIChomozygous50230932
124905276849052769TC22GENIChomozygous50230934
124905539549055396AC5GENIChomozygous50230936
124905566749055668GGA8GENICpossibly homozygous50230938
124905607749056078CCA8GENIChomozygous50230940
124905614649056147CA7GENIChomozygous50230942
124905572249055723TG3GENIChomozygous50513695
124905593049055933AAG---2GENIChomozygous50513697
124905616249056163AAGCTATTTCTTACTCCCAACTTCCCCGATGGGCACCCATTACCTGTTCCCTGCTGC7GENIChomozygous50513699