chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2056544595654460AAC9GENIChomozygous749094520
2056550655655066TC34GENIChomozygous637013188
2056555755655576CT30GENIChomozygous637013189
2056567935656794GA23GENIChomozygous637013190
2056569625656963AAGT21GENICheterozygous749094521
2056569625656963AAGTGT21GENICheterozygous749094522
2056574085657412TTAA----15GENICpossibly homozygous749094524
2056574425657443AG14GENIChomozygous637013191
2056579385657964TGTGTGTGTGTGTGTGTGTGTGTGTC--------------------------24GENICpossibly homozygous749094525
2056583765658377AG31GENIChomozygous637013192
2056589015658902TG11GENIChomozygous637013193
2056599715659994TTTTTTTTTCTTTTTTCTTTTTT-----------------------10GENICheterozygous749094526
2056602245660225TA12GENIChomozygous637013194
2056629025662903CT22GENIChomozygous637013195
2056637985663808GTGTGCGCGC----------8GENICheterozygous749094527
2056662905666291AATG22GENICpossibly homozygous749094528
2056665285666529AAT20GENIChomozygous749094530
2056686965668697G-23GENIChomozygous749094531
2056693135669314GT43GENIChomozygous637013196
2056706325670633GA36GENIChomozygous637013197
2056708145670815GA36GENIChomozygous637013198