chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
10108396361108396379GTGTGTGTGTGTGTGTGT------------------8GENICheterozygous52814155
10108396363108396379GTGTGTGTGTGTGTGT----------------8GENICheterozygous52814158
10108396766108396767TC62GENIChomozygous51596096
10108397090108397091GT13GENIChomozygous51596098
10108397871108397872CT78GENIChomozygous51596100
10108397987108397988CT40GENIChomozygous51596102
10108398368108398369AG55GENIChomozygous51596104
10108398863108398864TC53GENIChomozygous51596106
10108399592108399593CT30GENIChomozygous51596108
10108400449108400450AG51GENIChomozygous51596112
10108401443108401451GTGTGTGT--------14GENICheterozygous52331693
10108401486108401487TC23GENIChomozygous51596116
10108402283108402284AG38GENIChomozygous51596118
10108403550108403551TTAAC23GENIChomozygous51596120
10108403553108403554GGGGCTAC23GENIChomozygous51596122
10108403578108403590GAAAGAAAGAAA------------7GENIChomozygous52814161
10108403922108403924AA--32GENIChomozygous51596124
10108405663108405664TTC43GENIChomozygous51596126
10108406935108406936AAGT5GENICheterozygous51596128
10108407055108407057TT--6GENICheterozygous51596130
10108407075108407076TG8GENIChomozygous52271555
10108401441108401451GTGTGTGTGT----------14GENICheterozygous52734362
10108404773108404774GGGCACATAAACGTGTGTTCCCGTGGACCCGTGCTCACGA42GENIChomozygous52409529
10108407071108407072TG9GENIChomozygous52271553
10108407056108407057T-6GENICheterozygous52447870
10108407879108407880AT75GENICpossibly homozygous51596132
10108408876108408877AT7GENIChomozygous52409531
10108409222108409223AC13GENIChomozygous52409533
10108409485108409486AG17GENIChomozygous51596140
10108410258108410259TA55GENIChomozygous51596142
10108411238108411239GA22GENIChomozygous51596144
10108411944108411945GGCACACACACACACACACACACACACA16GENIChomozygous52409537
10108412065108412066GA44GENIChomozygous51596148
10108412067108412068CCT43GENIChomozygous51596149
10108412524108412525CT33GENIChomozygous51596151
10108412774108412775TC52GENIChomozygous51596153