chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
325301362530137AG29GENIChomozygous57136061
325306962530697AG39GENIChomozygous57136063
325323452532346AG36GENIChomozygous57136065
325326022532603TTTGCTTCCAGACAGGGGCTGTGCACAGGCTAACGTCCCCATGGCGACGC10GENIChomozygous59036054
325328262532827CT38GENIChomozygous57136067
325340282534029GA20GENIChomozygous57136069
325343662534367CA36GENIChomozygous57136071
325351232535124AG39GENIChomozygous57136073
325351362535137AG39GENIChomozygous57136075
325351502535151AG39GENIChomozygous57136077
325351572535158AG39GENIChomozygous57136079
325356502535651CT32GENIChomozygous57136081
325361182536119CG31GENICpossibly homozygous57136083
325365332536534AAGCACCCGGGGGCTG30GENIChomozygous57136087
325367632536764CA28GENICpossibly homozygous57136089
325368642536865AG16GENIChomozygous57136091
325372702537271CT20GENIChomozygous57136093
325376052537606CT30GENIChomozygous57136095
325376842537685CT37GENIChomozygous57136097
325381812538184AAA---10GENIChomozygous57136099
325387662538767AC35GENIChomozygous57136101
325400822540083GA37GENIChomozygous57136103
325400902540091TC36GENIChomozygous57136105
325401072540108AT36GENIChomozygous57136107
325401292540136TTTTTGG-------20GENIChomozygous57136109
325402742540275AT29GENIChomozygous57136111
325408032540804TC40GENIChomozygous57136113
325410482541080TGCTGATGCTGTGACATATAGGAAGGTGCTGA--------------------------------43GENICheterozygous58990563
325422132542214G-34GENIChomozygous57136127
325451552545156AATC14GENIChomozygous57136129
325489612548962GA32GENIChomozygous57136131