chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
10108396361108396379GTGTGTGTGTGTGTGTGT------------------17GENICheterozygous52814155
10108396363108396379GTGTGTGTGTGTGTGT----------------17GENICpossibly homozygous52814158
10108396766108396767TC40GENIChomozygous51596096
10108397090108397091GT30GENIChomozygous51596098
10108397871108397872CT36GENIChomozygous51596100
10108397987108397988CT41GENIChomozygous51596102
10108398368108398369AG29GENIChomozygous51596104
10108398863108398864TC27GENIChomozygous51596106
10108399592108399593CT32GENIChomozygous51596108
10108400449108400450AG37GENIChomozygous51596112
10108401441108401451GTGTGTGTGT----------10GENICheterozygous52734362
10108401443108401451GTGTGTGT--------10GENICpossibly homozygous52331693
10108401486108401487TC13GENIChomozygous51596116
10108402283108402284AG31GENIChomozygous51596118
10108403550108403551TTAAC24GENIChomozygous51596120
10108403553108403554GGGGCTAC22GENIChomozygous51596122
10108403578108403590GAAAGAAAGAAA------------6GENIChomozygous52814161
10108403922108403924AA--27GENIChomozygous51596124
10108404773108404774GGGCACATAAACGTGTGTTCCCGTGGACCCGTGCTCACGA24GENIChomozygous52409529
10108405663108405664TTC24GENIChomozygous51596126
10108406935108406936AAGT8GENICheterozygous51596128
10108407055108407057TT--6GENIChomozygous51596130
10108407071108407072TG8GENIChomozygous52271553
10108407075108407076TG8GENIChomozygous52271555
10108407879108407880AT32GENIChomozygous51596132
10108408876108408877AT20GENIChomozygous52409531
10108409222108409223AC12GENIChomozygous52409533
10108409485108409486AG26GENIChomozygous51596140
10108410258108410259TA35GENIChomozygous51596142
10108411238108411239GA35GENIChomozygous51596144
10108411944108411945GGCACACACACACACACACACACACACA7GENIChomozygous52409537
10108412065108412066GA30GENIChomozygous51596148
10108412067108412068CCT31GENIChomozygous51596149
10108412524108412525CT29GENIChomozygous51596151
10108412774108412775TC40GENIChomozygous51596153