chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
109039804990398050GA37GENIChomozygous116904589
109039806890398069CT39GENIChomozygous116904591
109039810490398105CA34GENIChomozygous116904593
109039874090398741TC26GENIChomozygous116904595
109039896290398963GA31GENIChomozygous116904597
109039935490399355TC23GENIChomozygous116904599
109039937390399374CT24GENIChomozygous116904601
109039940590399406CT29GENIChomozygous116904603
109040050090400501GT22GENIChomozygous116904605
109040050190400502GC22GENIChomozygous116676210
109040051090400511TC20GENIChomozygous116676212
109040507890405079CT22GENIChomozygous116904611
109040525290405253AC25GENIChomozygous116904613
109040652890406529GA28GENIChomozygous116904617
109040709390407094GC38GENIChomozygous116676216
109040721390407214AG35GENIChomozygous116904619
109040748590407486GA25GENIChomozygous116676218
109040857690408577TC26GENIChomozygous116904621
109040947890409479CT24GENIChomozygous116904623
109040990290409903GT30GENIChomozygous116676222
109041002490410025GA42GENIChomozygous116904625
109041420490414205CT40GENIChomozygous116904627
109041465090414651GA24GENIChomozygous116904629
109041491290414913TC31GENIChomozygous116904631
109041516390415164GA37GENIChomozygous116676236
109041539090415391AT37GENIChomozygous116676238