chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4146773041146773042CT57GENIChomozygous137226726
4146773309146773310CT47GENIChomozygous137226727
4146773598146773599GT55GENIChomozygous137226728
4146773869146773870TA40GENIChomozygous137226729
4146773872146773873TC40GENIChomozygous137226730
4146774054146774055T48GENIChomozygous136920019
4146774060146774061AG48GENIChomozygous137226731
4146774414146774415T40GENIChomozygous136920020
4146774440146774441GA42GENIChomozygous137226733
4146774676146774676TGAGCCATCGTGTCTTTAG49GENIChomozygous136920021
4146774680146774680T47GENIChomozygous136920022
4146774682146774682CTGT50GENIChomozygous136920023
4146775052146775053G55GENIChomozygous141588295
4146775052146775053GT55GENICheterozygous154224737
4146775095146775096TC55GENIChomozygous137226735
4146775119146775119A53GENIChomozygous136920024
4146775773146775774GA58GENIChomozygous137226736
4146775819146775820GA57GENIChomozygous137226737
4146776161146776162GA52GENIChomozygous137226738
4146776366146776367TC73GENIChomozygous137226739
4146776697146776698GA58GENIChomozygous137226740
4146776724146776725AG61GENIChomozygous137226741
4146776887146776888GA50GENIChomozygous137226742
4146776992146776993AG61GENIChomozygous137226743
4146777286146777287TC50GENIChomozygous141666539
4146777522146777523AG49GENIChomozygous137226744
4146777760146777761TC64GENIChomozygous137226745
4146777772146777773GA67GENIChomozygous141666540
4146778227146778228AG55GENIChomozygous137226747
4146779096146779097AG59GENIChomozygous137226748
4146779185146779186AG55GENIChomozygous137226749