chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
53317613933176140CT16GENIChomozygous934997014
53317705133177052AC22GENIChomozygous934997015
53317764233177643GA23GENICheterozygous934997016
53317766833177669CA26GENICheterozygous934997017
53317775133177752GT21GENICheterozygous934997018
53317777633177777TC25GENICheterozygous934997019
53317785333177854AG23GENICheterozygous934997020
53317815933178160CT22GENICheterozygous934997021
53317821033178211CG20GENICheterozygous934997022
53317821633178217GA16GENICheterozygous934997023
53317822133178222AG16GENICheterozygous934997024
53317822633178227AG16GENICheterozygous934997025
53317823133178232GT14GENICheterozygous934997026
53317964433179645AG9GENIChomozygous934997027
53318044233180443CT12GENIChomozygous934997028
53318066033180661TC4GENIChomozygous934997029