chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104548654845486550TT--18GENIChomozygous51442629
104548798245487983AT16GENIChomozygous51442630
104548853745488538GA24GENIChomozygous51442631
104548863145488632A-12GENIChomozygous51442633
104548894445488945GA18GENIChomozygous51442634
104548957345489574TA22GENIChomozygous51442635
104549053945490540TC43GENIChomozygous51442637
104549057745490578AG59GENIChomozygous51442638
104549057845490579AC59GENIChomozygous51442639
104549105345491054TC35GENIChomozygous51442640
104549112145491122GA49GENIChomozygous51442641
104549140845491409CT55GENIChomozygous51442642
104549141445491415AC56GENIChomozygous51442643
104549262945492630AC34GENIChomozygous51442644
104549280145492802AG49GENIChomozygous51442645
104549369445493696TT--8GENICheterozygous51442646
104549369545493696T-8GENICheterozygous51442647
104549561945495620GGACAC9GENIChomozygous51442648
104548788045487881T-4GENIChomozygous51636283
104549067845490679GA51GENIChomozygous51636284
104548978545489786TTCCTCTCTCTC13GENIChomozygous52373011
104549537545495376GGA47GENIChomozygous52373013
104549583945495840CG45GENIChomozygous51442649
104549692145496922TC57GENIChomozygous51442650
104549714245497143CCTT8GENIChomozygous51442651
104549755445497555CT64GENIChomozygous51442652
104549880245498803GA29GENIChomozygous51442653
104549941345499414GA42GENIChomozygous51442654
104549963645499637TTGAGA10GENICheterozygous52373019
104549976145499762TA42GENIChomozygous51442655
104550076145500762AG26GENIChomozygous51442656
104550132545501326TC38GENIChomozygous51442657
104550133545501336AT39GENIChomozygous51442658
104550199245501993GA37GENIChomozygous51442659
104550284745502851TGTG----6GENIChomozygous52496690
104550293345502937CTCT----22GENICheterozygous52052567
104550293545502937CT--22GENICheterozygous52722823
104550439245504393AAGAACAGCCACACCTTGGCATACACC45GENIChomozygous53332143