chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
175398329053983291CT6GENIChomozygous878621545
175398448153984482TC16GENIChomozygous878621546
175398519453985195AC15GENIChomozygous878621547
175398725053987251AG20GENIChomozygous878621548
175399097153990972TG3GENICheterozygous878621549
175399312053993121AC16GENIChomozygous878621550
175399390753993908GA17GENIChomozygous878621551
175399448553994486GA13GENIChomozygous878621552
175399712353997124AC5GENICheterozygous878621553
175399836253998363AT10GENIChomozygous878621554
175400060254000603AT16GENIChomozygous878621555
175400357954003580CA10GENIChomozygous878621556
175400402954004030GT15GENIChomozygous878621557
175400458654004587CA16GENIChomozygous878621558
175400976554009766GA12GENIChomozygous878621559
175401080154010802AG16GENIChomozygous878621560
175401097654010977CT20GENIChomozygous878621561
175401238554012386TC10GENIChomozygous878621562
175401650154016502GC6GENIChomozygous878621563
175401795154017952TC14GENIChomozygous878621564
175401848354018484CT20GENIChomozygous878621565
175402255854022559AG15GENIChomozygous878621566
175402314954023150CT12GENIChomozygous878621567
175402457954024580CT9GENIChomozygous878621568
175402475754024758AG14GENIChomozygous878621569