chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
514203361420336TCACTTTATCTCACTAGAGGTTTCTTTGTAAAGTGTCACGGAAATAGAAACTCCCTAAATATTAAGAGCTAACTGCATCATATTCAGGAAATCCAAGTCCATATGCTCAGATTCTTTTGTGCAAATTCTGATCTGTTATGCTTTTTTATAAACCTACTATAAAGCTATGGAAGATATCTAGGAAGACCCACTGTGCTATATATGTA48GENICpossibly homozygous128142886
514206361420637TA45GENIChomozygous113624826
514206591420660TA52GENIChomozygous113624828
514206681420669CA53GENIChomozygous113624830
514206721420673TA54GENIChomozygous113624832
514206801420681CA53GENIChomozygous113624834
514206921420693GA57GENIChomozygous113624836
514206931420694TA57GENIChomozygous114105644
514206961420697CA57GENIChomozygous113624838
514206991420700CA57GENIChomozygous113624840
514207031420704GA57GENIChomozygous113624842
514207141420715GT54GENIChomozygous113624844
514894001489401AG37GENICheterozygous122446079
514894081489409GA42GENICheterozygous132632325
514907471490748G28GENICheterozygous128142898
514907591490760AT30GENICheterozygous113625018
514908001490800C31GENICheterozygous128142899
514908781490879CA42GENICheterozygous114105663
514908911490891T38GENICheterozygous128142900
514894341489435CT42GENICheterozygous114663454
514913391491340GC43GENICheterozygous132080731
514914591491460AG28GENICheterozygous128278022
514916161491617GC47GENICheterozygous114105664
514916221491623TG47GENICheterozygous114105665
514916251491626CT49GENICheterozygous114105666
514917791491780TC41GENICheterozygous133400033
514920951492096TA35GENICheterozygous130757728
514921011492102CT37GENICheterozygous130757729