chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
106077138960771390TC34GENICheterozygous117130854
106077139960771400AG36GENICheterozygous117996380
106077140260771403GA38GENICheterozygous117996382
106077141360771414GC39GENICheterozygous117130855
106077145660771457GA40GENICheterozygous117996383
106077156060771561GA23GENIChomozygous117996386
106077163660771637GC24GENIChomozygous117219398
106077164760771648AG30GENICheterozygous117996388
106077163260771633AC32GENICheterozygous118067636
106077167560771676AG30GENICheterozygous118067637
106077160660771607CT30GENICheterozygous118067634
106077161660771617TC30GENICheterozygous118067635
106077167760771678AG30GENICheterozygous118067638
106077182760771828GT18GENIChomozygous117196162
106077187960771880CA20GENIChomozygous117219400
106077194960771950TC17GENIChomozygous117996389
106077197860771979GT14GENIChomozygous118067639
106077204560772046AG14GENIChomozygous117996391
106077211460772115GA22GENICpossibly homozygous117996392
106077220560772206TC20GENICpossibly homozygous117996394
106077228860772289AT23GENIChomozygous116890641