chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
108637041786370418AG44GENICpossibly homozygous51527982
108637060586370606CCT6GENICheterozygous51527983
108637080186370802AG52GENICheterozygous51527984
108637336286373364GG--10GENICheterozygous51527985
108637680186376802AACT51GENICheterozygous51527986
108637683186376832AACACACATT58GENICheterozygous51527987
108637690086376901TC116GENICheterozygous51527988
108637704186377042TA75GENICheterozygous51527989
108637708686377087C-46GENICheterozygous51527990
108638294886382949TTACACAC19GENICpossibly homozygous51527991
108639109086391091TTGG14GENICheterozygous51527992
108639109486391098TTTT----4GENICheterozygous51527993