chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
105353128953531290TTA13GENICpossibly homozygous51648397
105353175553531756AG28GENIChomozygous51648398
105353424153534242AG29GENIChomozygous51648400
105353502853535029T-22GENIChomozygous51648401
105353548653535487GA28GENIChomozygous51648403
105353565953535660TC19GENIChomozygous51648404
105354757753547578TC28GENIChomozygous51648418
105355068853550689TC21GENIChomozygous52057578
105353965253539653GGT8GENICpossibly homozygous52057572
105353787353537874GGTC17GENICpossibly homozygous52460357
105355083553550836GA36GENIChomozygous52057580
105355096453550983CATGCGGTTACTCATCCAA-------------------16GENIChomozygous52057582
105355100953551010GA15GENIChomozygous52057584
105355106653551067TA12GENIChomozygous52057586
105355112353551124GGTCA21GENIChomozygous52057588
105355114553551146TC21GENIChomozygous52057590
105355116053551161GA22GENIChomozygous52057592
105355125553551256GA26GENIChomozygous51648421
105355129553551296A-20GENICpossibly homozygous52057598
105355129853551309GTGTGTGTGTG-----------10GENICpossibly homozygous52460358
105355129853551299G-10GENICheterozygous52460359
105355137853551379GA5GENIChomozygous52460360
105355169953551700TA22GENIChomozygous52057610
105355170153551702AG21GENIChomozygous52318756
105355185653551857GC22GENIChomozygous52057612
105355185953551860GA22GENIChomozygous52057614
105355186253551863TG21GENIChomozygous52057616
105355207953552081TT--21GENIChomozygous52057618
105355242853552429GA21GENIChomozygous52057622
105355247353552474AG20GENIChomozygous52057624
105355307153553072GT34GENIChomozygous52057630
105355250853552509AATG21GENICpossibly homozygous52057626
105355297253552973AG26GENIChomozygous52057628
105355307253553073AT31GENIChomozygous52057632
105355311753553118T-25GENIChomozygous52057634
105355370653553707A-26GENIChomozygous51455619
105355372953553730AC26GENIChomozygous51455620