chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2160180921160180922GC13GENIChomozygous59188535
2160180923160180924GC13GENIChomozygous59188536
2160180953160180954TC6GENICheterozygous59188537
2160180955160180956TC5GENIChomozygous59188538
2160181387160181388TC47GENIChomozygous60147984
2160181956160181970ACACGTCTCTTCCC--------------14GENIChomozygous60147986
2160181957160181958CCAA16GENICheterozygous60147988
2160181960160181961GGC13GENICheterozygous60147990
2160182271160182272TC34GENIChomozygous59188543
2160183308160183309GT40GENIChomozygous60147992
2160183644160183645GA35GENIChomozygous60147993
2160185130160185131C-8GENICpossibly homozygous60147995
2160185663160185664AAT19GENIChomozygous59188545
2160188285160188286AT13GENICheterozygous59188548
2160189015160189016GT34GENIChomozygous60147997
2160189497160189498CCG13GENIChomozygous60147999
2160192308160192309AAT23GENICheterozygous59188549
2160192310160192311CT25GENICpossibly homozygous60148001
2160192557160192558TC29GENIChomozygous59188550
2160192915160192916CG41GENIChomozygous59188551
2160193038160193039CT46GENIChomozygous59188552
2160193334160193335GT11GENIChomozygous59188553
2160193422160193423TTC2GENIChomozygous59188554
2160193470160193471GT62GENICheterozygous59890048
2160193668160193669CT22GENICheterozygous59188556
2160194006160194007TC47GENIChomozygous59188557
2160194365160194366GT35GENIChomozygous59188558
2160194808160194809GA36GENIChomozygous59188559
2160196006160196007AC33GENIChomozygous59188562
2160196659160196660TA31GENICpossibly homozygous60148003
2160197090160197091GA29GENIChomozygous59188563
2160197182160197184AA--10GENIChomozygous59890051
2160197200160197201G-16GENICheterozygous59188564
2160198687160198688G-33GENIChomozygous59188570
2160200211160200212TC22GENIChomozygous59188574
2160200459160200460GA35GENIChomozygous60148005
2160201497160201498TC28GENICheterozygous59763244