chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
10108396766108396767TC27GENIChomozygous51596096
10108397090108397091GT17GENIChomozygous51596098
10108397871108397872CT39GENIChomozygous51596100
10108398368108398369AG23GENIChomozygous51596104
10108398863108398864TC27GENIChomozygous51596106
10108399592108399593CT13GENIChomozygous51596108
10108400449108400450AG16GENIChomozygous51596112
10108401486108401487TC13GENIChomozygous51596116
10108402283108402284AG25GENIChomozygous51596118
10108403550108403551TTAAC23GENIChomozygous51596120
10108403553108403554GGGGCTAC23GENIChomozygous51596122
10108403922108403924AA--23GENIChomozygous51596124
10108405663108405664TTC27GENIChomozygous51596126
10108406307108406308CT24GENIChomozygous52271551
10108401449108401451GT--9GENIChomozygous52409525
10108403570108403590GAAAGAAAGAAAGAAAGAAA--------------------4GENIChomozygous52409527
10108404773108404774GGGCACATAAACGTGTGTTCCCGTGGACCCGTGCTCACGA40GENIChomozygous52409529
10108401484108401485TC12GENIChomozygous52271543
10108402257108402258CT27GENIChomozygous52271545
10108402268108402269AT28GENIChomozygous52271547
10108403116108403117AG35GENIChomozygous52271549
10108407071108407072TG13GENICheterozygous52271553
10108407075108407076TG15GENICpossibly homozygous52271555
10108407879108407880AT35GENIChomozygous51596132
10108408876108408877AT11GENIChomozygous52409531
10108409222108409223AC17GENIChomozygous52409533
10108409485108409486AG29GENIChomozygous51596140
10108410258108410259TA28GENIChomozygous51596142
10108411944108411945GGCACACACACACACACACACACACACA7GENIChomozygous52409537
10108412065108412066GA17GENIChomozygous51596148
10108412067108412068CCT17GENIChomozygous51596149
10108412524108412525CT20GENIChomozygous51596151
10108412774108412775TC35GENIChomozygous51596153
10108407056108407057T-6GENICheterozygous52447870
10108406936108406944GTGTGTGT--------6GENIChomozygous52216626