chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
414878361487837AG11GENIChomozygous113073160
414878481487849AC11GENIChomozygous112462708
414880851488086CG5GENIChomozygous113326603
414882081488209AG8GENIChomozygous113073162
414882141488215TA6GENIChomozygous113073163
414882261488227TG6GENIChomozygous113073164
414883751488376CA17GENIChomozygous113073165
414884891488490AG8GENIChomozygous113073166
414884971488498TG5GENIChomozygous113073167
414885251488526GA6GENIChomozygous113073168
414886671488668TG15GENIChomozygous113073169
414887131488714TG12GENIChomozygous113073170
414887381488739TC9GENIChomozygous113073171
414887391488740GA8GENIChomozygous113073172
414888341488835AG25GENIChomozygous113073173
414888981488899TG6GENIChomozygous113073174
414889501488951GA28GENICheterozygous113073175
414890031489004CT13GENIChomozygous113073176
414890191489020AG8GENICheterozygous113073177
414890201489021CT4GENICheterozygous126038964
414891581489159AC22GENIChomozygous113073179
414892411489242CT10GENICheterozygous125999338
414891421489143TC13GENICheterozygous125999333
414891781489179TA11GENICheterozygous125999335
414893401489341TA21GENICheterozygous113073181
414894001489401GT23GENIChomozygous113073182
414894251489426AG13GENICheterozygous126038965
414895131489514CG16GENIChomozygous113073183
414899111489912GA5GENIChomozygous126140404
414893781489379TG10GENICheterozygous126045062