chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2160180726160180729TTT---2GENICheterozygous60755830
2160180727160180729TT--2GENICheterozygous60503966
2160180921160180922GC4GENIChomozygous59188535
2160180923160180924GC4GENIChomozygous59188536
2160180952160180953AAC7GENIChomozygous60503967
2160181387160181388TC20GENIChomozygous60147984
2160181956160181970ACACGTCTCTTCCC--------------21GENIChomozygous60147986
2160182271160182272TC21GENIChomozygous59188543
2160183308160183309GT26GENIChomozygous60147992
2160183644160183645GA22GENIChomozygous60147993
2160185130160185131C-5GENIChomozygous60147995
2160185663160185664AAT21GENIChomozygous59188545
2160188292160188294GA--3GENIChomozygous60503968
2160189015160189016GT28GENIChomozygous60147997
2160192310160192311CT17GENIChomozygous60148001
2160192557160192558TC30GENIChomozygous59188550
2160192915160192916CG14GENIChomozygous59188551
2160193038160193039CT17GENIChomozygous59188552
2160193334160193335GT8GENIChomozygous59188553
2160193422160193423TTC2GENIChomozygous59188554
2160193668160193669CT22GENIChomozygous59188556
2160194006160194007TC19GENIChomozygous59188557
2160194365160194366GT17GENIChomozygous59188558
2160194808160194809GA22GENIChomozygous59188559
2160196006160196007AC12GENIChomozygous59188562
2160196659160196660TA22GENIChomozygous60148003
2160197090160197091GA20GENIChomozygous59188563
2160197182160197184AA--4GENICheterozygous59890051
2160198687160198688G-29GENIChomozygous59188570
2160200211160200212TC25GENIChomozygous59188574
2160200459160200460GA25GENIChomozygous60148005