chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4146773041146773042CT32GENIChomozygous137226726
4146773309146773310CT32GENIChomozygous137226727
4146773598146773599GT45GENIChomozygous137226728
4146773869146773870TA63GENIChomozygous137226729
4146773872146773873TC63GENIChomozygous137226730
4146774054146774055T46GENIChomozygous136920019
4146774060146774061AG46GENIChomozygous137226731
4146774414146774415T27GENICpossibly homozygous136920020
4146774440146774441GA38GENIChomozygous137226733
4146774676146774676TGAGCCATCGTGTCTTTAG38GENIChomozygous136920021
4146774680146774680T38GENIChomozygous136920022
4146774682146774682CTGT39GENIChomozygous136920023
4146775052146775053G42GENICpossibly homozygous141588295
4146775095146775096TC45GENIChomozygous137226735
4146775119146775119A43GENIChomozygous136920024
4146775773146775774GA51GENIChomozygous137226736
4146775819146775820GA48GENIChomozygous137226737
4146776161146776162GA56GENIChomozygous137226738
4146776366146776367TC56GENIChomozygous137226739
4146776697146776698GA56GENICpossibly homozygous137226740
4146776724146776725AG58GENIChomozygous137226741
4146776887146776888GA47GENIChomozygous137226742
4146776992146776993AG59GENIChomozygous137226743
4146779096146779097AG52GENIChomozygous137226748
4146777522146777523AG58GENIChomozygous137226744
4146777760146777761TC59GENICpossibly homozygous137226745
4146778227146778228AG47GENIChomozygous137226747
4146777286146777287TC41GENICpossibly homozygous141666539
4146777772146777773GA65GENICpossibly homozygous141666540
4146779185146779186AG45GENIChomozygous137226749