chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
91430518314305184TC17GENIChomozygous51762446
91430587514305876TC15GENIChomozygous52843399
91430772514307726CA21GENIChomozygous52843401
91430826014308261CT3GENIChomozygous51762474
91430870514308706AG7GENICheterozygous52843404
91430910214309103G-13GENIChomozygous52843406
91431193414311935GA19GENIChomozygous52843411
91431380514313806TA22GENICpossibly homozygous52843414
91431421214314213G-10GENICheterozygous51762496
91431433114314332AATGCT6GENICheterozygous52843417
91431433514314340CCCCC-----4GENIChomozygous52843420
91431460114314602CT28GENICpossibly homozygous52843423