chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
10108396361108396379GTGTGTGTGTGTGTGTGT------------------8GENICheterozygous52814155
10108396363108396379GTGTGTGTGTGTGTGT----------------8GENICheterozygous52814158
10108396766108396767TC22GENIChomozygous51596096
10108397090108397091GT34GENIChomozygous51596098
10108397871108397872CT26GENIChomozygous51596100
10108397987108397988CT24GENIChomozygous51596102
10108398368108398369AG10GENIChomozygous51596104
10108398863108398864TC18GENIChomozygous51596106
10108399592108399593CT22GENIChomozygous51596108
10108400449108400450AG10GENIChomozygous51596112
10108401443108401451GTGTGTGT--------7GENICheterozygous52331693
10108401486108401487TC17GENICpossibly homozygous51596116
10108402283108402284AG20GENIChomozygous51596118
10108403550108403551TTAAC29GENIChomozygous51596120
10108403553108403554GGGGCTAC29GENIChomozygous51596122
10108403578108403590GAAAGAAAGAAA------------4GENIChomozygous52814161
10108403922108403924AA--16GENIChomozygous51596124
10108405663108405664TTC26GENIChomozygous51596126
10108406935108406936AAGT11GENICpossibly homozygous51596128
10108407055108407057TT--21GENICheterozygous51596130
10108407056108407057T-21GENICheterozygous52447870
10108407071108407072TG28GENIChomozygous52271553
10108407075108407076TG26GENIChomozygous52271555
10108407879108407880AT27GENIChomozygous51596132
10108401441108401451GTGTGTGTGT----------7GENICheterozygous52734362
10108404773108404774GGGCACATAAACGTGTGTTCCCGTGGACCCGTGCTCACGA39GENIChomozygous52409529
10108408876108408877AT16GENICpossibly homozygous52409531
10108409222108409223AC20GENIChomozygous52409533
10108409485108409486AG34GENIChomozygous51596140
10108410258108410259TA17GENIChomozygous51596142
10108411238108411239GA30GENIChomozygous51596144
10108411944108411945GGCACACACACACACACACACACACACA3GENIChomozygous52409537
10108412065108412066GA25GENIChomozygous51596148
10108412067108412068CCT25GENIChomozygous51596149
10108412524108412525CT39GENIChomozygous51596151
10108412774108412775TC16GENIChomozygous51596153