chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
58032598380325984AG20GENIChomozygous55489308
58032636280326363CA35GENIChomozygous55489310
58032653780326538GGA39GENIChomozygous55489312
58032665380326654GA20GENIChomozygous55489314
58032668280326683CCCG10GENIChomozygous55489316
58032669380326707TACACACACACACA--------------12GENICheterozygous55886929
58032675180326757GGGGGA------5GENIChomozygous55489318
58032686180326862C-35GENIChomozygous55489320
58032710880327109AG17GENIChomozygous55489322
58032715980327160TG29GENIChomozygous55489324
58032723680327237CG39GENIChomozygous55489326
58032748680327497CCTGGGCAGTC-----------13GENIChomozygous55489328
58032805080328051CCACAA9GENIChomozygous55489330
58032805480328055CA12GENICheterozygous55489332
58032855280328553GA46GENIChomozygous55489334
58032857580328576AT50GENIChomozygous55489336
58032861480328615TC54GENIChomozygous55489338
58032967780329678GGGCGGCGA8GENIChomozygous55489340
58032986280329870CACTGTGT--------8GENIChomozygous55489342
58032999480329995GA21GENIChomozygous55489344
58033022480330225GT30GENIChomozygous55489346
58033022580330226AT31GENIChomozygous55489348
58033037080330376TGTGTG------1GENIChomozygous55489350
58033044280330443AG35GENICpossibly homozygous55489352
58033102380331024TC25GENIChomozygous55489354