chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101015470010154701TC29GENIChomozygous51323997
101015506510155066CT23GENIChomozygous51323998
101015669210156693AG14GENIChomozygous51324001
101015677410156775AG13GENIChomozygous51324002
101015680510156806GGT10GENICpossibly homozygous51324003
101015680510156806GGTT10GENICheterozygous51324004
101015701510157017TT--5GENICheterozygous52480737
101015701610157017T-5GENICheterozygous52718611
101015706510157066AAC7GENIChomozygous51324007
101015717810157179GGTGTA16GENIChomozygous51324008
101015754910157550CT21GENIChomozygous51324010
101015982110159822GA28GENIChomozygous51324011
101016125210161253CCA11GENICheterozygous51616360
101016171910161720GA23GENIChomozygous51324012
101016206410162065CT14GENIChomozygous51324013
101016330910163310GA34GENIChomozygous51324016
101016353310163534TC21GENIChomozygous51324017
101016422310164224GGAA14GENICheterozygous51324018
101016422310164224GGA14GENICpossibly homozygous51324019
101016294710162963GTGTGTGTGCGCGCGC----------------12GENICheterozygous52795897