chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
10108396363108396379GTGTGTGTGTGTGTGT----------------8GENICpossibly homozygous52814158
10108396766108396767TC27GENIChomozygous51596096
10108397090108397091GT47GENIChomozygous51596098
10108397871108397872CT28GENIChomozygous51596100
10108397987108397988CT32GENIChomozygous51596102
10108398368108398369AG23GENIChomozygous51596104
10108398863108398864TC18GENIChomozygous51596106
10108399592108399593CT26GENIChomozygous51596108
10108400449108400450AG25GENIChomozygous51596112
10108401486108401487TC15GENIChomozygous51596116
10108402283108402284AG25GENIChomozygous51596118
10108403550108403551TTAAC36GENIChomozygous51596120
10108403553108403554GGGGCTAC37GENIChomozygous51596122
10108403922108403924AA--25GENIChomozygous51596124
10108404773108404774GGGCACATAAACGTGTGTTCCCGTGGACCCGTGCTCACGA41GENIChomozygous52409529
10108405663108405664TTC24GENIChomozygous51596126
10108406935108406936AAGT5GENICheterozygous51596128
10108407055108407057TT--9GENIChomozygous51596130
10108407071108407072TG14GENIChomozygous52271553
10108407075108407076TG17GENIChomozygous52271555
10108407879108407880AT34GENIChomozygous51596132
10108408876108408877AT22GENIChomozygous52409531
10108409222108409223AC24GENIChomozygous52409533
10108409485108409486AG31GENIChomozygous51596140
10108410258108410259TA30GENIChomozygous51596142
10108411238108411239GA28GENIChomozygous51596144
10108411944108411945GGCACACACACACACACACACACACACA4GENIChomozygous52409537
10108412065108412066GA24GENIChomozygous51596148
10108412067108412068CCT23GENIChomozygous51596149
10108412524108412525CT26GENIChomozygous51596151
10108412774108412775TC26GENIChomozygous51596153