chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
121970408619704087TA6GENIChomozygous890364015
121970420619704207TG12GENIChomozygous890364016
121970487919704880GT9GENIChomozygous890364017
121970490519704906TC15GENICheterozygous890364018
121970492119704922GA17GENICheterozygous890364019
121970494419704945AT19GENIChomozygous890364020
121970511919705120GT19GENIChomozygous890364021
121970514919705150AG11GENIChomozygous890364022
121970595119705952TC16GENIChomozygous890364023
121970602219706023CT13GENIChomozygous890364024
121970610919706110TC19GENICheterozygous890364025
121970611019706111CT19GENICheterozygous890364026
121970650619706507AT15GENIChomozygous890364027
121970703219707033CT11GENIChomozygous890364028
121970704519707046CT13GENICheterozygous890364029
121970717919707180AC7GENIChomozygous890364030
121970751619707517GA12GENIChomozygous890364031
121970754019707541AT8GENIChomozygous890364032
121970756519707566CG10GENICheterozygous890364033
121970801019708011CT12GENIChomozygous890364034
121970804819708049CA5GENIChomozygous890364035