chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
98188058281880583AG18GENIChomozygous117586684
98188179281881793TC14GENIChomozygous117586692
98188577581885776AG26GENIChomozygous117586706
98188654281886543AG21GENIChomozygous117586708
98188761681887617TA11GENIChomozygous120279572
98189007181890072AG17GENIChomozygous117586718
98189039681890397CA18GENIChomozygous117586720
98189112781891128AC5GENIChomozygous120428097
98189126281891263AG20GENIChomozygous117586726
98189376581893766AG24GENIChomozygous117586742
98189480681894807AG27GENIChomozygous117586758
98189596381895964AG26GENIChomozygous117586770
98189657281896573CT25GENIChomozygous120279575
98189717181897172CT20GENIChomozygous120279576
98189831881898319AG18GENIChomozygous117586794
98189896981898970TC19GENIChomozygous117586802
98189926781899268AG24GENIChomozygous117586804
98189930381899304TC20GENIChomozygous117586806
98190013981900140CT26GENIChomozygous120279577
98190071581900716TC26GENIChomozygous117586814
98190076481900765TC33GENIChomozygous117586816
98190089081900891TC17GENIChomozygous117586818
98190090881900909TC14GENIChomozygous117586820
98190215781902158CT5GENIChomozygous120279578
98190218081902181TC3GENIChomozygous120279579
98190260681902607TA9GENIChomozygous120279581
98190433781904338TC21GENIChomozygous120279584
98190451981904520TC15GENIChomozygous117586846
98190479181904792AC7GENIChomozygous120279585
98190543281905433AT28GENIChomozygous120279586
98190598481905985TC23GENIChomozygous120279587
98190645381906454GA7GENIChomozygous120279588
98190683381906834AG12GENIChomozygous120279589
98190773381907734CT2GENIChomozygous120279590