chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
69980591599805916AT19GENIChomozygous115141479
69980682599806826TC12GENICpossibly homozygous114916097
69980709499807095GA18GENIChomozygous114916098
69980713699807137GC19GENIChomozygous114916099
69980733699807337AG8GENIChomozygous114916100
69980743299807433CT8GENIChomozygous114916101
69980759499807595GA19GENIChomozygous115141480
69980768599807686GT23GENIChomozygous115469911
69980823199808232CA12GENICheterozygous114916103
69980826299808263TC15GENIChomozygous114916104
69980884799808848AG19GENIChomozygous114916105
69980912499809125TC23GENIChomozygous114916106
69980944799809448CT22GENIChomozygous114916107
69980969799809698AC19GENIChomozygous115141481
69980977599809776GA24GENIChomozygous114916108
69981021699810217TC13GENICpossibly homozygous114916109
69981074699810747GA11GENICpossibly homozygous114916110
69981083099810831GT20GENIChomozygous114916111
69981093299810933GA11GENIChomozygous114916112
69981093899810939GA12GENIChomozygous114916113