chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
10108396361108396379GTGTGTGTGTGTGTGTGT------------------18GENICheterozygous52814155
10108396363108396379GTGTGTGTGTGTGTGT----------------18GENICheterozygous52814158
10108396766108396767TC48GENIChomozygous51596096
10108397090108397091GT29GENIChomozygous51596098
10108397871108397872CT37GENIChomozygous51596100
10108397987108397988CT39GENIChomozygous51596102
10108398368108398369AG36GENIChomozygous51596104
10108398863108398864TC59GENIChomozygous51596106
10108399592108399593CT15GENIChomozygous51596108
10108400449108400450AG50GENIChomozygous51596112
10108401441108401451GTGTGTGTGT----------12GENICheterozygous52734362
10108401443108401451GTGTGTGT--------12GENICheterozygous52331693
10108401486108401487TC29GENICpossibly homozygous51596116
10108402283108402284AG45GENIChomozygous51596118
10108403550108403551TTAAC28GENIChomozygous51596120
10108403553108403554GGGGCTAC27GENIChomozygous51596122
10108403578108403590GAAAGAAAGAAA------------5GENIChomozygous52814161
10108403922108403924AA--31GENIChomozygous51596124
10108405663108405664TTC52GENIChomozygous51596126
10108406935108406936AAGT5GENIChomozygous51596128
10108407055108407057TT--7GENICheterozygous51596130
10108407071108407072TG11GENIChomozygous52271553
10108407075108407076TG11GENIChomozygous52271555
10108407879108407880AT40GENIChomozygous51596132
10108409485108409486AG33GENIChomozygous51596140
10108410258108410259TA37GENIChomozygous51596142
10108411238108411239GA35GENIChomozygous51596144
10108404773108404774GGGCACATAAACGTGTGTTCCCGTGGACCCGTGCTCACGA54GENIChomozygous52409529
10108408876108408877AT38GENIChomozygous52409531
10108409222108409223AC11GENIChomozygous52409533
10108407056108407057T-7GENICheterozygous52447870
10108411944108411945GGCACACACACACACACACACACACACA8GENIChomozygous52409537
10108412065108412066GA39GENIChomozygous51596148
10108412067108412068CCT40GENIChomozygous51596149
10108412524108412525CT40GENIChomozygous51596151
10108412774108412775TC38GENIChomozygous51596153