chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
10108396355108396379GTGTGTGTGTGTGTGTGTGTGTGT------------------------14GENICpossibly homozygous52331691
10108396469108396470AG25GENIChomozygous51953747
10108396766108396767TC28GENIChomozygous51596096
10108396843108396844GA29GENIChomozygous51953750
10108397090108397091GT15GENIChomozygous51596098
10108397341108397342TC28GENIChomozygous51953753
10108397389108397390GA30GENIChomozygous51953756
10108398923108398924CT35GENIChomozygous51953759
10108399390108399391AG22GENIChomozygous51953762
10108399592108399593CT26GENIChomozygous51596108
10108400014108400015CCTCT22GENIChomozygous51953766
10108400065108400066CA27GENIChomozygous51953772
10108401441108401451GTGTGTGTGT----------11GENICheterozygous52734362
10108401443108401451GTGTGTGT--------11GENICpossibly homozygous52331693
10108401486108401487TC18GENIChomozygous51596116
10108402283108402284AG27GENIChomozygous51596118
10108403425108403426GA29GENIChomozygous51953778
10108403550108403551TTAAC29GENIChomozygous51596120
10108403553108403554GGGGCTAC29GENIChomozygous51596122
10108403570108403590GAAAGAAAGAAAGAAAGAAA--------------------5GENIChomozygous52409527
10108404773108404774GGGCACATAAACGTGTGTTCCCGTGGACCCGTGCTCACGA42GENIChomozygous52409529
10108405663108405664TTC25GENIChomozygous51596126
10108406942108406944GT--7GENIChomozygous52734364
10108407056108407057T-12GENIChomozygous52447870
10108407067108407068TG15GENIChomozygous52734366
10108407071108407072TG13GENIChomozygous52271553
10108407075108407076TG12GENIChomozygous52271555
10108409222108409223A-9GENIChomozygous51953784
10108409223108409224AC9GENIChomozygous52734368
10108409485108409486AG27GENIChomozygous51596140
10108411960108411961AACGCACGCGCGCG6GENIChomozygous52734370
10108411969108411970CCACACACACACACACACACAT15GENIChomozygous52331695
10108412067108412068CCT26GENIChomozygous51596149
10108412524108412525CT24GENIChomozygous51596151
10108412774108412775TC27GENIChomozygous51596153