chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5140644040140644041TC44GENIChomozygous114030705
5140644151140644152AG46GENIChomozygous114030706
5140644415140644463CGCACGCATGCACGCACGCATGCACGCACGCATGCACGCACGCATGCA35GENIChomozygous131650770
5140648010140648011TC47GENIChomozygous114030713
5140648494140648495GA47GENIChomozygous114251083
5140647738140647739AG42GENIChomozygous114251079
5140647920140647921GT47GENICpossibly homozygous114251081
5140649127140649128TC43GENIChomozygous114030716
5140649856140649857GA57GENIChomozygous114251085
5140651082140651083TC74GENIChomozygous114030722
5140651278140651279TC56GENIChomozygous114030724
5140651285140651286TC61GENIChomozygous114030725
5140651974140651975CT55GENIChomozygous114251089
5140652571140652572CT51GENIChomozygous114251091
5140652635140652636TC35GENIChomozygous114030726
5140652873140652874CT54GENIChomozygous114030727
5140653387140653388G32GENIChomozygous128246909
5140653474140653475GA49GENIChomozygous114030728
5140653736140653737G28GENIChomozygous128246910
5140653740140653741TC29GENIChomozygous114030730
5140653749140653749GAGGAGGAG28GENIChomozygous128246911
5140654163140654164AG43GENIChomozygous114030731
5140654249140654250AG26GENIChomozygous114030733
5140654307140654308AG16GENIChomozygous114030735
5140654737140654739TT38GENIChomozygous128246912
5140654803140654804CT42GENIChomozygous114251095
5140655331140655332TC67GENIChomozygous114251097
5140655332140655333GA66GENIChomozygous114251099
5140655363140655364CT61GENIChomozygous114251101
5140655668140655669AG51GENIChomozygous114030739
5140655917140655918AC54GENIChomozygous114251103
5140656403140656404GA54GENIChomozygous114251105
5140656424140656425CA56GENIChomozygous114251107
5140656866140656866AATGGTTT29GENIChomozygous132079139
5140657006140657007AT17GENIChomozygous114251109
5140657064140657065CA44GENIChomozygous114251111
5140657356140657357TG56GENIChomozygous114251113
5140657642140657643TC65GENIChomozygous114251115
5140657661140657662GA64GENIChomozygous114251117