chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4146773041146773042CT60GENIChomozygous137226726
4146773309146773310CT31GENIChomozygous137226727
4146773598146773599GT50GENIChomozygous137226728
4146773869146773870TA51GENIChomozygous137226729
4146773872146773873TC51GENIChomozygous137226730
4146774054146774055T49GENIChomozygous136920019
4146774060146774061AG52GENIChomozygous137226731
4146774195146774196AG56GENIChomozygous137226732
4146774414146774415T44GENIChomozygous136920020
4146774676146774676TGAGCCATCGTGTCTTTAG56GENIChomozygous136920021
4146774680146774680T52GENIChomozygous136920022
4146774682146774682CTGT51GENIChomozygous136920023
4146775119146775119A53GENIChomozygous136920024
4146776161146776162GA59GENIChomozygous137226738
4146774440146774441GA49GENIChomozygous137226733
4146775050146775051TA35GENICpossibly homozygous137226734
4146775095146775096TC55GENIChomozygous137226735
4146775773146775774GA52GENIChomozygous137226736
4146775819146775820GA64GENIChomozygous137226737
4146775052146775053G35GENICheterozygous141588295
4146775052146775053GT35GENICpossibly homozygous154224737
4146776366146776367TC63GENIChomozygous137226739
4146776697146776698GA53GENIChomozygous137226740
4146776724146776725AG55GENIChomozygous137226741
4146776887146776888GA52GENIChomozygous137226742
4146776992146776993AG62GENIChomozygous137226743
4146777522146777523AG63GENIChomozygous137226744
4146777760146777761TC41GENIChomozygous137226745
4146777926146777927GA69GENIChomozygous137226746
4146778227146778228AG62GENIChomozygous137226747
4146779096146779097AG47GENIChomozygous137226748
4146779185146779186AG46GENIChomozygous137226749