chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4168873032168873033GC13GENIChomozygous113475866
4168873970168873971GA21GENIChomozygous113475868
4168874069168874070TC24GENIChomozygous113475870
4168874080168874081TC21GENIChomozygous113475872
4168875484168875485GA12GENIChomozygous113475874
4168875519168875520CT11GENIChomozygous113475876
4168876811168876812GA25GENIChomozygous113475878
4168877391168877392TG23GENIChomozygous113475880
4168877424168877425GC28GENIChomozygous113475882
4168880436168880437AG21GENIChomozygous113475884
4168880650168880651CT25GENICheterozygous113067676
4168880883168880884GA24GENIChomozygous113475886
4168881130168881131AG27GENIChomozygous113475888
4168881769168881770CT12GENIChomozygous113475890
4168881814168881815TC10GENIChomozygous112945481
4168881864168881865TC16GENIChomozygous113475892
4168881998168881999GC15GENIChomozygous113475894
4168882366168882367GA13GENIChomozygous113475896
4168882554168882555CT22GENIChomozygous113475898
4168882581168882582GA29GENICpossibly homozygous113475900
4168883561168883562CT18GENIChomozygous112945483
4168884477168884478TC15GENIChomozygous112945485