chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
25850682658506827GT18GENIChomozygous978164108
25850694858506949TA16GENIChomozygous978164109
25850713758507138CT29GENIChomozygous978164110
25850719158507192CA24GENIChomozygous978164111
25850723658507237AC27GENIChomozygous978164112
25850740458507405AT15GENIChomozygous978164113
25850789958507900GA29GENIChomozygous978164114
25850953958509540TG47GENIChomozygous978164115
25851059358510594AG38GENIChomozygous978164116
25851065758510658TC42GENIChomozygous978164117
25851082158510822TG39GENIChomozygous978164118
25851154758511548TC76GENIChomozygous978164119
25851181958511820AC38GENIChomozygous978164120
25851235458512355AT50GENICpossibly homozygous978164121
25851275058512751TC17GENIChomozygous978164122
25851296358512964GA37GENIChomozygous978164123
25851303858513039GA36GENIChomozygous978164124
25851306858513069CT51GENIChomozygous978164125
25851604958516050CA50GENIChomozygous978164126
25851938958519390CT40GENIChomozygous978164127
25851976458519765TC29GENIChomozygous978164128
25851984858519849TA33GENIChomozygous978164129
25851994958519950TC30GENIChomozygous978164130
25852153858521539CA27GENIChomozygous978164131
25852187058521871GC51GENIChomozygous978164132
25852189558521896TC41GENIChomozygous978164133
25852192058521921AG38GENIChomozygous978164134
25852229558522296GC47GENIChomozygous978164135
25852259358522594GA40GENIChomozygous978164136
25852278258522783GA34GENIChomozygous978164137
25852281158522812CT42GENIChomozygous978164138
25852293458522935CT49GENIChomozygous978164139
25852305158523052TC34GENIChomozygous978164140
25852654058526541CT25GENIChomozygous978164141
25853184058531841TC22GENIChomozygous978164142
25853188358531884TC32GENIChomozygous978164143