chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1271687380271687381CA9GENICheterozygous61220569
1271687603271687604GA18GENICpossibly homozygous61220571
1271687614271687615CT13GENICpossibly homozygous61220573
1271688650271688651CT9GENICpossibly homozygous61220575
1271688805271688806GA9GENIChomozygous61645292
1271690898271690899TC28GENICpossibly homozygous61220583
1271691122271691123CCCCT1GENIChomozygous61220585
1271691963271691964GGTGTGTGTGTGTA8GENICheterozygous62305493
1271692187271692188AG23GENIChomozygous61220601
1271692945271692963ACAACAACAACAACAACA------------------1GENIChomozygous61645293
1271693180271693181GA9GENICpossibly homozygous61220607
1271693464271693465CCTT1GENIChomozygous61220609
1271693599271693600TC24GENIChomozygous61220611
1271694080271694081GA25GENICpossibly homozygous61220613
1271695474271695475AG23GENICpossibly homozygous61220617
1271698258271698259TC10GENIChomozygous61220627
1271704768271704769CT3GENIChomozygous61645298
1271704890271704891TC14GENIChomozygous61645299
1271705494271705495TTG3GENICheterozygous61645300
1271705887271705888CT20GENICpossibly homozygous61645301
1271707281271707282TC17GENIChomozygous61645302