chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
414878361487837AG22GENIChomozygous113073160
414878481487849AC19GENIChomozygous112462708
414879471487948GA25GENIChomozygous113073161
414882081488209AG23GENIChomozygous113073162
414882141488215TA22GENIChomozygous113073163
414882261488227TG22GENIChomozygous113073164
414883751488376CA23GENIChomozygous113073165
414884891488490AG26GENIChomozygous113073166
414884971488498TG25GENIChomozygous113073167
414885251488526GA24GENIChomozygous113073168
414886671488668TG31GENIChomozygous113073169
414887131488714TG35GENIChomozygous113073170
414887381488739TC27GENIChomozygous113073171
414887391488740GA27GENIChomozygous113073172
414888341488835AG38GENIChomozygous113073173
414888981488899TG30GENIChomozygous113073174
414889501488951GA43GENIChomozygous113073175
414890031489004CT37GENIChomozygous113073176
414890191489020AG39GENIChomozygous113073177
414890661489067TA27GENIChomozygous113073178
414891581489159AC33GENICpossibly homozygous113073179
414892971489298CG30GENIChomozygous113073180
414893401489341TA24GENIChomozygous113073181
414894001489401GT21GENIChomozygous113073182
414895131489514CG23GENIChomozygous113073183
414896481489649GA21GENIChomozygous112462711
414897041489705CG22GENIChomozygous113073184
414897071489708GC21GENIChomozygous113073185