chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
16067875760678758GA22GENIChomozygous60723081
16067889460678895TC22GENIChomozygous60723082
16067908260679083TC18GENIChomozygous60723083
16067940260679403AG16GENIChomozygous60723084
16067950460679505AG9GENIChomozygous60723085
16067952260679523TC7GENIChomozygous60723086
16067960060679601CT9GENIChomozygous60723087
16067973160679732GA12GENICheterozygous60723088
16067982660679827A-9GENIChomozygous60723089
16068011560680116AG10GENIChomozygous60723090
16068150160681502AT19GENIChomozygous60723091
16068158660681587A-2GENIChomozygous61703641
16068195360681954CG21GENICpossibly homozygous60723092
16068219560682196GA9GENIChomozygous60723093
16068225060682251GA13GENIChomozygous60723094
16068259160682592CT15GENIChomozygous60723097
16068267160682672AC24GENICpossibly homozygous60723098
16068319460683195GT22GENICpossibly homozygous60723099
16068356260683676TAGATTCCTTTTTGTTTTTTTTTTTCTTTTTCTATTTTTCGGAGCTGGGGACTGAACCCAGGGCCTTGCGCTTGGTAGGCAAGCGCTCTACCACTGAGCTAAATCCCCAACCCT------------------------------------------------------------------------------------------------------------------8GENICheterozygous62129361
16068398560683986CT21GENICpossibly homozygous60723100
16068410560684106GA15GENICheterozygous60723101
16068416360684164CG16GENIChomozygous60723102
16068436760684368CA6GENIChomozygous60723103
16068456960684570GA31GENICpossibly homozygous60723104
16068536460685365AG20GENIChomozygous60723105
16068643760686438AC13GENIChomozygous60723106
16068665760686658CT9GENICpossibly homozygous60723107