chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
175398329053983291CT16GENIChomozygous881693754
175398448153984482TC16GENIChomozygous881693755
175398519453985195AC13GENIChomozygous881693756
175398725053987251AG17GENIChomozygous881693757
175398810953988110CT9GENICheterozygous881693758
175399312053993121AC29GENIChomozygous881693759
175399347153993472GC8GENIChomozygous881693760
175399390753993908GA29GENIChomozygous881693761
175399448553994486GA24GENIChomozygous881693762
175399836253998363AT17GENIChomozygous881693763
175400060254000603AT21GENIChomozygous881693764
175400357954003580CA9GENIChomozygous881693765
175400402954004030GT19GENIChomozygous881693766
175400437254004373AG20GENIChomozygous881693767
175400458654004587CA11GENIChomozygous881693768
175400539354005394AG11GENIChomozygous881693769
175400976554009766GA13GENIChomozygous881693770
175401080154010802AG25GENIChomozygous881693771
175401097654010977CT21GENIChomozygous881693772
175401238554012386TC10GENIChomozygous881693773
175401650154016502GC6GENICheterozygous881693774
175401795154017952TC24GENIChomozygous881693775
175401848354018484CT13GENIChomozygous881693776
175402255854022559AG21GENIChomozygous881693777
175402314954023150CT14GENIChomozygous881693778
175402457954024580CT5GENIChomozygous881693779
175402475754024758AG15GENIChomozygous881693780